<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Archiving and Interchange DTD with MathML3 v1.3 20210610//EN"  "JATS-archivearticle1-3-mathml3.dtd"><article xmlns:ali="http://www.niso.org/schemas/ali/1.0/" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" article-type="research-article" dtd-version="1.3"><front><journal-meta><journal-id journal-id-type="nlm-ta">elife</journal-id><journal-id journal-id-type="publisher-id">eLife</journal-id><journal-title-group><journal-title>eLife</journal-title></journal-title-group><issn publication-format="electronic" pub-type="epub">2050-084X</issn><publisher><publisher-name>eLife Sciences Publications, Ltd</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">96997</article-id><article-id pub-id-type="doi">10.7554/eLife.96997</article-id><article-id pub-id-type="doi" specific-use="version">10.7554/eLife.96997.3</article-id><article-version article-version-type="publication-state">version of record</article-version><article-categories><subj-group subj-group-type="display-channel"><subject>Research Article</subject></subj-group><subj-group subj-group-type="heading"><subject>Neuroscience</subject></subj-group></article-categories><title-group><article-title>Value construction through sequential sampling explains serial dependencies in decision making</article-title></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name><surname>Zylberberg</surname><given-names>Ariel</given-names></name><contrib-id authenticated="true" contrib-id-type="orcid">https://orcid.org/0000-0002-2572-4748</contrib-id><email>ariel.zylberberg@gmail.com</email><xref ref-type="aff" rid="aff1">1</xref><xref ref-type="fn" rid="con1"/><xref ref-type="fn" rid="conf1"/></contrib><contrib contrib-type="author"><name><surname>Bakkour</surname><given-names>Akram</given-names></name><xref ref-type="aff" rid="aff1">1</xref><xref ref-type="aff" rid="aff2">2</xref><xref ref-type="aff" rid="aff3">3</xref><xref ref-type="other" rid="fund5"/><xref ref-type="fn" rid="con2"/><xref ref-type="fn" rid="conf1"/></contrib><contrib contrib-type="author" equal-contrib="yes"><name><surname>Shohamy</surname><given-names>Daphna</given-names></name><xref ref-type="aff" rid="aff1">1</xref><xref ref-type="aff" rid="aff4">4</xref><xref ref-type="aff" rid="aff5">5</xref><xref ref-type="fn" rid="equal-contrib1">†</xref><xref ref-type="other" rid="fund4"/><xref ref-type="other" rid="fund6"/><xref ref-type="other" rid="fund7"/><xref ref-type="fn" rid="con3"/><xref ref-type="fn" rid="conf1"/></contrib><contrib contrib-type="author" equal-contrib="yes"><name><surname>Shadlen</surname><given-names>Michael N</given-names></name><contrib-id authenticated="true" contrib-id-type="orcid">https://orcid.org/0000-0002-2002-2210</contrib-id><xref ref-type="aff" rid="aff1">1</xref><xref ref-type="aff" rid="aff4">4</xref><xref ref-type="aff" rid="aff6">6</xref><xref ref-type="aff" rid="aff7">7</xref><xref ref-type="fn" rid="equal-contrib1">†</xref><xref ref-type="other" rid="fund1"/><xref ref-type="other" rid="fund2"/><xref ref-type="other" rid="fund3"/><xref ref-type="fn" rid="con4"/><xref ref-type="fn" rid="conf1"/></contrib><aff id="aff1"><label>1</label><institution-wrap><institution-id institution-id-type="ror">https://ror.org/00hj8s172</institution-id><institution>Mortimer B Zuckerman Mind Brain Behavior Institute, Columbia University</institution></institution-wrap><addr-line><named-content content-type="city">New York</named-content></addr-line><country>United States</country></aff><aff id="aff2"><label>2</label><institution-wrap><institution-id institution-id-type="ror">https://ror.org/024mw5h28</institution-id><institution>Department of Psychology, University of Chicago</institution></institution-wrap><addr-line><named-content content-type="city">Chicago</named-content></addr-line><country>United States</country></aff><aff id="aff3"><label>3</label><institution-wrap><institution-id institution-id-type="ror">https://ror.org/024mw5h28</institution-id><institution>Neuroscience Institute, University of Chicago</institution></institution-wrap><addr-line><named-content content-type="city">Chicago</named-content></addr-line><country>United States</country></aff><aff id="aff4"><label>4</label><institution-wrap><institution-id institution-id-type="ror">https://ror.org/00hj8s172</institution-id><institution>Department of Neuroscience, Columbia University</institution></institution-wrap><addr-line><named-content content-type="city">New York</named-content></addr-line><country>United States</country></aff><aff id="aff5"><label>5</label><institution-wrap><institution-id institution-id-type="ror">https://ror.org/00hj8s172</institution-id><institution>Department of Psychology, Columbia University</institution></institution-wrap><addr-line><named-content content-type="city">New York</named-content></addr-line><country>United States</country></aff><aff id="aff6"><label>6</label><institution-wrap><institution-id institution-id-type="ror">https://ror.org/00hj8s172</institution-id><institution>The Kavli Institute for Brain Science, Columbia University</institution></institution-wrap><addr-line><named-content content-type="city">New York</named-content></addr-line><country>United States</country></aff><aff id="aff7"><label>7</label><institution-wrap><institution-id institution-id-type="ror">https://ror.org/006w34k90</institution-id><institution>Howard Hughes Medical Institute</institution></institution-wrap><addr-line><named-content content-type="city">Chevy Chase</named-content></addr-line><country>United States</country></aff></contrib-group><contrib-group content-type="section"><contrib contrib-type="editor"><name><surname>Donner</surname><given-names>Tobias H</given-names></name><role>Reviewing Editor</role><aff><institution-wrap><institution-id institution-id-type="ror">https://ror.org/01zgy1s35</institution-id><institution>University Medical Center Hamburg-Eppendorf</institution></institution-wrap><country>Germany</country></aff></contrib><contrib contrib-type="senior_editor"><name><surname>Frank</surname><given-names>Michael J</given-names></name><role>Senior Editor</role><aff><institution-wrap><institution-id institution-id-type="ror">https://ror.org/05gq02987</institution-id><institution>Brown University</institution></institution-wrap><country>United States</country></aff></contrib></contrib-group><author-notes><fn fn-type="con" id="equal-contrib1"><label>†</label><p>These authors contributed equally to this work</p></fn></author-notes><pub-date publication-format="electronic" date-type="publication"><day>10</day><month>12</month><year>2024</year></pub-date><volume>13</volume><elocation-id>RP96997</elocation-id><history><date date-type="sent-for-review" iso-8601-date="2024-04-02"><day>02</day><month>04</month><year>2024</year></date></history><pub-history><event><event-desc>This manuscript was published as a preprint.</event-desc><date date-type="preprint" iso-8601-date="2024-01-15"><day>15</day><month>01</month><year>2024</year></date><self-uri content-type="preprint" xlink:href="https://doi.org/10.1101/2024.01.13.575363"/></event><event><event-desc>This manuscript was published as a reviewed preprint.</event-desc><date date-type="reviewed-preprint" iso-8601-date="2024-05-23"><day>23</day><month>05</month><year>2024</year></date><self-uri content-type="reviewed-preprint" xlink:href="https://doi.org/10.7554/eLife.96997.1"/></event><event><event-desc>The reviewed preprint was revised.</event-desc><date date-type="reviewed-preprint" iso-8601-date="2024-11-18"><day>18</day><month>11</month><year>2024</year></date><self-uri content-type="reviewed-preprint" xlink:href="https://doi.org/10.7554/eLife.96997.2"/></event></pub-history><permissions><copyright-statement>© 2024, Zylberberg et al</copyright-statement><copyright-year>2024</copyright-year><copyright-holder>Zylberberg et al</copyright-holder><ali:free_to_read/><license xlink:href="http://creativecommons.org/licenses/by/4.0/"><ali:license_ref>http://creativecommons.org/licenses/by/4.0/</ali:license_ref><license-p>This article is distributed under the terms of the <ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by/4.0/">Creative Commons Attribution License</ext-link>, which permits unrestricted use and redistribution provided that the original author and source are credited.</license-p></license></permissions><self-uri content-type="pdf" xlink:href="elife-96997-v1.pdf"/><self-uri content-type="figures-pdf" xlink:href="elife-96997-figures-v1.pdf"/><abstract><p>Deciding between a pair of familiar items is thought to rely on a comparison of their subjective values. When the values are similar, decisions take longer, and the choice may be inconsistent with stated value. These regularities are thought to be explained by the same mechanism of noisy evidence accumulation that leads to perceptual errors under conditions of low signal to noise. However, unlike perceptual decisions, subjective values may vary with internal states (e.g. desires, priorities) that change over time. This raises the possibility that the apparent stochasticity of choice reflects changes in value rather than mere noise. We hypothesized that these changes would manifest in serial dependencies across decision sequences. We analyzed data from a task in which participants chose between snack items. We developed an algorithm, <italic>Reval</italic>, that revealed significant fluctuations of the subjective values of items within an experimental session. The dynamic values predicted choices and response times more accurately than stated values. The dynamic values also furnished a superior account of the BOLD signal in ventromedial prefrontal cortex. A novel bounded-evidence accumulation model with temporally correlated evidence samples supports the idea that revaluation reflects the dynamic construction of subjective value during deliberation, which in turn influences subsequent decisions.</p></abstract><kwd-group kwd-group-type="author-keywords"><kwd>decision making</kwd><kwd>value-based decisions</kwd><kwd>drift-diffusion model</kwd><kwd>choice-induced preference change</kwd><kwd>vmPFC</kwd><kwd>food-choice task</kwd></kwd-group><kwd-group kwd-group-type="research-organism"><title>Research organism</title><kwd>Human</kwd></kwd-group><funding-group><award-group id="fund1"><funding-source><institution-wrap><institution-id institution-id-type="FundRef">http://dx.doi.org/10.13039/100000002</institution-id><institution>National Institutes of Health</institution></institution-wrap></funding-source><award-id>R01NS113113</award-id><principal-award-recipient><name><surname>Shadlen</surname><given-names>Michael N</given-names></name></principal-award-recipient></award-group><award-group id="fund2"><funding-source><institution-wrap><institution-id institution-id-type="FundRef">http://dx.doi.org/10.13039/100000181</institution-id><institution>Air Force Office of Scientific Research</institution></institution-wrap></funding-source><award-id>FA9550-22-1-0337</award-id><principal-award-recipient><name><surname>Shadlen</surname><given-names>Michael N</given-names></name></principal-award-recipient></award-group><award-group id="fund3"><funding-source><institution-wrap><institution-id institution-id-type="FundRef">http://dx.doi.org/10.13039/100000011</institution-id><institution>Howard Hughes Medical Institute</institution></institution-wrap></funding-source><principal-award-recipient><name><surname>Shadlen</surname><given-names>Michael N</given-names></name></principal-award-recipient></award-group><award-group id="fund4"><funding-source><institution-wrap><institution-id institution-id-type="FundRef">http://dx.doi.org/10.13039/100005270</institution-id><institution>McKnight Foundation</institution></institution-wrap></funding-source><principal-award-recipient><name><surname>Shohamy</surname><given-names>Daphna</given-names></name></principal-award-recipient></award-group><award-group id="fund5"><funding-source><institution-wrap><institution-id institution-id-type="FundRef">http://dx.doi.org/10.13039/100000001</institution-id><institution>National Science Foundation</institution></institution-wrap></funding-source><award-id>1606916</award-id><principal-award-recipient><name><surname>Bakkour</surname><given-names>Akram</given-names></name></principal-award-recipient></award-group><award-group id="fund6"><funding-source><institution-wrap><institution-id institution-id-type="FundRef">http://dx.doi.org/10.13039/100000001</institution-id><institution>National Science Foundation</institution></institution-wrap></funding-source><award-id>1822619</award-id><principal-award-recipient><name><surname>Shohamy</surname><given-names>Daphna</given-names></name></principal-award-recipient></award-group><award-group id="fund7"><funding-source><institution-wrap><institution-id institution-id-type="FundRef">http://dx.doi.org/10.13039/100000002</institution-id><institution>National Institutes of Health</institution></institution-wrap></funding-source><award-id>MH121093</award-id><principal-award-recipient><name><surname>Shohamy</surname><given-names>Daphna</given-names></name></principal-award-recipient></award-group><funding-statement>The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.</funding-statement></funding-group><custom-meta-group><custom-meta specific-use="meta-only"><meta-name>Author impact statement</meta-name><meta-value>The subjective value of choice options changes during deliberation, and accounting for these changes improves predictions of choices, response times, and BOLD fMRI activity.</meta-value></custom-meta><custom-meta specific-use="meta-only"><meta-name>publishing-route</meta-name><meta-value>prc</meta-value></custom-meta></custom-meta-group></article-meta></front><body><sec id="s1" sec-type="intro"><title>Introduction</title><p>A central idea in decision theory and economics is that each good can be assigned a scalar utility value that reflects its desirability. The concept of utility, or subjective value, provides a common currency for comparing dissimilar goods (e.g. pears and apples) such that decision-making can be reduced to estimating the utility of each good and comparing them (<xref ref-type="bibr" rid="bib75">von Neumann and Morgenstern, 1944</xref>; <xref ref-type="bibr" rid="bib61">Samuelson, 1937</xref>; <xref ref-type="bibr" rid="bib52">Montague and Berns, 2002</xref>). The idea is supported by studies that have identified neurons that correlate with the subjective value of alternatives in various brain structures, most notably the ventromedial prefrontal cortex, and it is so pervasive that decisions based on preferences are often referred to as ‘value-based decisions’ (<xref ref-type="bibr" rid="bib39">Kable and Glimcher, 2007</xref>; <xref ref-type="bibr" rid="bib42">Kim et al., 2008</xref>; <xref ref-type="bibr" rid="bib54">Padoa-Schioppa and Assad, 2006</xref>).</p><p>Choice and response time (RT) in simple perceptual and mnemonic decisions are often modeled within the framework of bounded evidence accumulation (BEA). The framework posits that evidence samples for and against the different options are accumulated over time until the accumulated evidence for one of the options reaches a threshold or bound (<xref ref-type="bibr" rid="bib58">Ratcliff, 1978</xref>; <xref ref-type="bibr" rid="bib26">Gold and Shadlen, 2007</xref>). A case in point is the random dot motion (RDM) discrimination task, in which participants must decide whether randomly moving dots have net rightward or leftward motion, while the experimenter controls the proportion of dots moving coherently in one direction, termed the <italic>motion strength</italic> (e.g. <xref ref-type="bibr" rid="bib26">Gold and Shadlen, 2007</xref>). BEA models explain the choice, RT, and confidence in the RDM task under the assumption that the rate of accumulation, often termed the <italic>drift rate</italic>, depends on motion strength (<xref ref-type="bibr" rid="bib72">van den Berg et al., 2016</xref>; <xref ref-type="bibr" rid="bib81">Zylberberg and Shadlen, 2024</xref>). Value-based decisions have also been modeled within the framework of BEA. The key assumption is that at any given time, decision-makers only have access to a noisy representation of the subjective value of each item, and the drift rate depends on the difference between the subjective values of the items (<xref ref-type="bibr" rid="bib44">Krajbich et al., 2010</xref>; <xref ref-type="bibr" rid="bib69">Thomas et al., 2019</xref>; <xref ref-type="bibr" rid="bib63">Sepulveda et al., 2020</xref>; <xref ref-type="bibr" rid="bib5">Bakkour et al., 2019</xref>).</p><p>A condition that renders the BEA framework normative is that the noise corrupting the evidence samples is independent, or equivalently, that the evidence samples are conditionally independent given the drift rate. For example, in modeling the RDM and other perceptual decision making tasks, evidence samples are assumed to be independent of each other, conditioned on motion strength and direction (e.g. <xref ref-type="bibr" rid="bib78">Zylberberg et al., 2016</xref>). This assumption is sensible because (<italic>i</italic>) the main source of stochasticity in perceptual decision making is the noise affecting the sensory representation of the evidence, which has a short-lived autocorrelation, and (<italic>ii</italic>) these decisions are often based on an evidence stream (e.g. a dynamic random dot display) that provides conditionally independent samples, by design. The assumption of conditional independence justifies the process of evidence accumulation, because accumulation (or averaging) can only remove the noise components that are not shared by the evidence samples.</p><p>For value-based decisions, the assumption of conditional independence is questionable. Alternatives often differ across multiple attributes (e.g. <xref ref-type="bibr" rid="bib13">Busemeyer and Townsend, 1993</xref>; <xref ref-type="bibr" rid="bib71">Tversky, 1977</xref>). For example, when choosing between different snacks, they may differ in calories, healthiness, palatability, and so on (<xref ref-type="bibr" rid="bib68">Suzuki et al., 2017</xref>). The weight given to each attribute depends on the decision-maker’s internal state (<xref ref-type="bibr" rid="bib53">Noguchi and Stewart, 2018</xref>; <xref ref-type="bibr" rid="bib38">Juechems and Summerfield, 2019</xref>). This internal state includes desires, needs, priorities, attentional state and goals. We use the term mindset, or state of mind, to refer to all these internal influences on valuation. A mindset can be persistent. For example, a famished decision-maker may prioritize the nutritional content of each food when making a choice. Under less pressing circumstances, the salience of an attribute may be suggested by snack alternatives themselves. For example, seeing French fries may make us aware that we crave something salty, and saltiness becomes a relevant attribute informing the current decision and possibly future decisions too. The examples illustrate how a decision-maker’s mindset can shift rapidly or meander, based on the attributes in focus or the identity of the items under consideration (<xref ref-type="bibr" rid="bib64">Shadlen and Shohamy, 2016</xref>; <xref ref-type="bibr" rid="bib67">Stewart et al., 2006</xref>). Importantly, mindset is dynamic. It can change abruptly, motivated by a thought in an earlier trial or by interoception during deliberation (e.g. thirst). Unlike perceptual decision-making, where the expectation of a sample of evidence is thought to be fixed, conditional on the stimulus, the expectation of the evidence bearing on preference is itself potentially dynamic.</p><p>We sought to test the notion that the desirability of an item changes as a result of the deliberation that leads to a choice. We hypothesized that if subjective values are dynamic, then value-based decisions should exhibit serial dependencies when multiple decisions are made in a sequence. A choice provides information not only about which option is preferred, but also about the decision maker’s mindset at the moment of the choice (e.g. whether they prioritize satiation or palatability). Therefore, a choice is informative about future choices because the decision maker’s <italic>mindset</italic> is likely to endure longer than a single decision, or even multiple decisions.</p><p>We reanalyzed data from <xref ref-type="bibr" rid="bib5">Bakkour et al., 2019</xref>. Participants were presented with pairs of snacks and had to choose the one they preferred. This <italic>Food choice task</italic> has been used extensively to study the sequential sampling process underlying value-based decisions (e.g. <xref ref-type="bibr" rid="bib44">Krajbich et al., 2010</xref>). Crucially, in the <xref ref-type="bibr" rid="bib5">Bakkour et al., 2019</xref> experiment, each item was presented multiple times, allowing us to infer how preference for an item changes during a single experimental session. Using a novel algorithm we call <italic>Reval</italic>, we show that the subjective value of items changed over the session. The revaluation was replicated in a sequential sampling model in which successive samples of evidence are not assumed to be conditionally independent. We argue that the revaluation process we observed reflects a process by which the value of the alternatives is constructed during deliberation by querying memory and prospecting for evidence that bears on desirability (<xref ref-type="bibr" rid="bib50">Lichtenstein and Slovic, 2006</xref>; <xref ref-type="bibr" rid="bib37">Johnson et al., 2007</xref>).</p></sec><sec id="s2" sec-type="results"><title>Results</title><sec id="s2-1"><title>Food choice task</title><p>We re-examined data from a previous study in which 30 participants completed a food choice task (<xref ref-type="bibr" rid="bib5">Bakkour et al., 2019</xref>). Prior to the main experiment, participants were asked to indicate their willingness to pay for each of 60 snack items on a scale from 0 to US$3 (<xref ref-type="fig" rid="fig1">Figure 1A</xref>). We refer to these explicitly reported values as <italic>s-values</italic>, or <inline-formula><mml:math id="inf1"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msub><mml:mi>v</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>s</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula> (where <inline-formula><mml:math id="inf2"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>s</mml:mi></mml:mstyle></mml:math></inline-formula> stands for ‘static’ as opposed to the ‘dynamic’ values we define below). In the main experiment (conducted in an MRI scanner), participants were shown pairs of images of previously rated snack items and had to choose which snack they would prefer to consume at the end of the study (<xref ref-type="fig" rid="fig1">Figure 1B</xref>).</p><fig id="fig1" position="float"><label>Figure 1.</label><caption><title>Food choice task.</title><p>(<bold>A</bold>) In an initial ‘ratings’ task, participants were shown 60 individual appetizing snack items and asked to indicate how much they would be willing to pay for each item using a monetary scale ranging from $0 to $3. (<bold>B</bold>) In the main experiment, participants were presented with pairs of snack items and asked to choose which one they would prefer to consume at the end of the session. After making their choice, the chosen item was highlighted by a square box for an additional 0.5 s. Each of the 30 participants completed 210 trials, with each item appearing seven times during the experiment. A subset of 60 item pairs were repeated once. (<bold>C</bold>) Proportion of trials in which participants selected the right item as a function of the difference in value between the right and left items (<inline-formula><mml:math id="inf3"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>s</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula>). Proportions were first determined for each participant and then averaged across participants. Error bars indicate the s.e.m. across participants. (<bold>D</bold>) Mean response time as a function of the difference in value between the right and left items. Error bars indicate the s.e.m. across participants. Red curves in panels C-D are fits of a drift-diffusion model (DDM).</p></caption><graphic mimetype="image" mime-subtype="tiff" xlink:href="elife-96997-fig1-v1.tif"/></fig><p>The data from <xref ref-type="bibr" rid="bib5">Bakkour et al., 2019</xref> replicate the behavior typically observed in such tasks. Both choice and response time were systematically related to the difference in <italic>s-value</italic>, <inline-formula><mml:math id="inf4"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>s</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula>, between the right and left items. Participants were more likely to choose the item to which they assigned a higher value during the rating phase (p&lt;0.0001; <inline-formula><mml:math id="inf5"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msub><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi class="MJX-tex-caligraphic" mathvariant="script">H</mml:mi></mml:mrow><mml:mrow class="MJX-TeXAtom-ORD"><mml:mn>0</mml:mn></mml:mrow></mml:msub><mml:mspace width="negativethinmathspace"/><mml:mo>:</mml:mo><mml:msub><mml:mi>β</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mn>1</mml:mn></mml:mrow></mml:msub><mml:mo>=</mml:mo><mml:mn>0</mml:mn></mml:mstyle></mml:math></inline-formula>; <xref ref-type="disp-formula" rid="equ2">Equation 2</xref>). They were also more likely to respond faster when the absolute value of the difference between the items, <inline-formula><mml:math id="inf6"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mrow><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mrow><mml:mo stretchy="false">|</mml:mo></mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow><mml:mi>s</mml:mi></mml:mrow></mml:msub><mml:mrow><mml:mo stretchy="false">|</mml:mo></mml:mrow></mml:mstyle></mml:mrow></mml:mstyle></mml:math></inline-formula>, was greater (p&lt;0.0001; <inline-formula><mml:math id="inf7"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msub><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi class="MJX-tex-caligraphic" mathvariant="script">H</mml:mi></mml:mrow><mml:mrow class="MJX-TeXAtom-ORD"><mml:mn>0</mml:mn></mml:mrow></mml:msub><mml:mspace width="negativethinmathspace"/><mml:mo>:</mml:mo><mml:msub><mml:mi>β</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mn>1</mml:mn></mml:mrow></mml:msub><mml:mo>=</mml:mo><mml:mn>0</mml:mn></mml:mstyle></mml:math></inline-formula>; <xref ref-type="disp-formula" rid="equ3">Equation 3</xref>).</p><p>The relationship between <inline-formula><mml:math id="inf8"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>s</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula>, choice, and response time is well described by a bounded evidence accumulation model (<xref ref-type="bibr" rid="bib44">Krajbich et al., 2010</xref>; <xref ref-type="bibr" rid="bib5">Bakkour et al., 2019</xref>). The solid lines in <xref ref-type="fig" rid="fig1">Figure 1C–D</xref> illustrate the fit of such a model in which the drift rate depends on <inline-formula><mml:math id="inf9"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>s</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula>. Overall, the behavior of our participants in the task is similar to that observed in other studies using the same task (e.g. <xref ref-type="bibr" rid="bib44">Krajbich et al., 2010</xref>; <xref ref-type="bibr" rid="bib24">Folke et al., 2016</xref>; <xref ref-type="bibr" rid="bib63">Sepulveda et al., 2020</xref>).</p></sec><sec id="s2-2"><title>Limited power of explicit reports of value to explain binary choices</title><p>An intriguing aspect of the decision process in the food choice task is its highly stochastic nature. This is evident from the shallowness of the choice function (<xref ref-type="fig" rid="fig1">Figure 1C</xref>): participants chose the item with a higher <italic>s-value</italic> in only 64% of the trials. This variability is typically attributed to unspecified noise when recalling item values from memory (e.g. <xref ref-type="bibr" rid="bib44">Krajbich et al., 2010</xref>). An alternative explanation is rooted in constructive value theories, which suggest that the value of each item is constructed, not retrieved, during the decision process (<xref ref-type="bibr" rid="bib50">Lichtenstein and Slovic, 2006</xref>; <xref ref-type="bibr" rid="bib64">Shadlen and Shohamy, 2016</xref>; <xref ref-type="bibr" rid="bib37">Johnson et al., 2007</xref>). This construction process is sensitive to the context in which it is elicited (e.g. the identity of items being compared), so the values reported during the valuation process may differ from those used in the choice task. According to this idea, the apparently stochastic choice is a veridical reflection of the constructed values.</p><p>If this were true, then the choice on any one <italic>cynosure</italic> trial—that is, the trial we are scrutinizing—would be better explained by values inferred from the choices on the other trials than by the <italic>s-values</italic>. We therefore compared two regression models that produce the log odds of the choice on each <italic>cynosure</italic> trial. The first regression model uses the <italic>s-values</italic> plus a potential bias for the left or right item. The second regression model includes one regression coefficient per item plus a left/right bias. It uses all the other trials (except repetitions of the identical pair of items) to establish the weights. While this model has more free parameters, the comparison is valid because we are using the models to predict the choices made on trials that were not used for model fitting. The better model is the one that produces larger log odds of the choice on the <italic>cynosure</italic> trial. As shown in <xref ref-type="fig" rid="fig2">Figure 2</xref>, the second regression model is superior.</p><fig id="fig2" position="float"><label>Figure 2.</label><caption><title>Individual choices are better explained by values inferred from the other trials than values reported in the ratings task.</title><p>Gray data points represent the total log-likelihood of each participant’s choices, given two types of predictions: (<italic>abscissa</italic>) from a logistic regression, fit to the static values; (<italic>ordinate</italic>) from a procedure that infers the values based on choices on the other trials. Predictions derived from the other trials are better in all but four participants. The red markers were obtained using the same procedure, applied to choices simulated under the assumption that the <italic>s-values</italic> are the true values of the items. It shows that the inferential procedure is not guaranteed to improve predictions.</p></caption><graphic mimetype="image" mime-subtype="tiff" xlink:href="elife-96997-fig2-v1.tif"/></fig><p>To ensure that this result is not produced artifactually from the algorithm, we performed the same analysis on simulated data. We fit the experimentally observed choices using a logistic regression model with <inline-formula><mml:math id="inf10"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>s</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula> and an offset as independent variables, and simulated the choices by sampling from Bernoulli distributions with parameter, <inline-formula><mml:math id="inf11"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>p</mml:mi></mml:mstyle></mml:math></inline-formula>, specified by the logistic function that best fit each participant’s choices (i.e., weighted-coin flips). We repeated the model comparison using the simulated choices and found that, contrary to what we observed in the experimental data, the model using explicit value reports is the better predictor (<xref ref-type="fig" rid="fig2">Figure 2</xref>, red).</p><p>Taken together, these analyses show that explicit value reports have limited power to predict choices, which partially explains their apparent stochasticity (<xref ref-type="bibr" rid="bib43">Konovalov and Krajbich, 2019</xref>; <xref ref-type="bibr" rid="bib73">Verhoef and Franses, 2003</xref>; <xref ref-type="bibr" rid="bib76">Wardman, 1988</xref>). In the following sections, we elaborate on this observation. Not only do the values used to make the binary choices differ from the <italic>s-values</italic>, they drift apart during the experiment. We show that these changes arise through the deliberative process leading to the preference decisions themselves.</p></sec><sec id="s2-3"><title>Preferences change over the course of the experiment</title><p>In the experiment, a subset of snack pairs were presented twice, in a random order within the sequence of trials. These trials allow us to assess whether preferences change over the course of a session. For these duplicated item pairs, we calculate the average number of times that the same item was chosen on both presentations—which we refer to as the <italic>match probability</italic>. Participants were more likely to select the same option when presentations of the same pair were closer in time (<xref ref-type="fig" rid="fig3">Figure 3</xref>). To assess the significance of this effect, we fit a logistic regression model using all pairs of trials with identical stimuli to predict the probability that the same item would be chosen on both occasions. The regression coefficient associated with the number of trials between repetitions was negative and highly significant (p&lt;0.0001; t-test, <xref ref-type="disp-formula" rid="equ8">Equation 8</xref>). It therefore follows that preferences are not fixed, not even over the course of a single experimental session.</p><fig id="fig3" position="float"><label>Figure 3.</label><caption><title>Preferences change over time.</title><p>Probability of making the same choice on the two trials with the same item pair, shown as a function of the difference in trial number between them (<inline-formula><mml:math id="inf12"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi mathvariant="normal">t</mml:mi><mml:mi mathvariant="normal">r</mml:mi></mml:mrow></mml:mstyle></mml:math></inline-formula>). Trial pairs with identical items (N=1726) were sorted by <inline-formula><mml:math id="inf13"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi mathvariant="normal">t</mml:mi><mml:mi mathvariant="normal">r</mml:mi></mml:mrow></mml:mstyle></mml:math></inline-formula>, and the match probabilities were smoothed with a boxcar function with a width of 100 observations.</p></caption><graphic mimetype="image" mime-subtype="tiff" xlink:href="elife-96997-fig3-v1.tif"/></fig></sec><sec id="s2-4"><title>Choice alternatives undergo revaluation</title><p>We propose a simple algorithm to characterize how preferences changed over the course of the session. It assumes that on each decision, the value of the chosen item increases by an amount equal to <inline-formula><mml:math id="inf14"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>δ</mml:mi></mml:mstyle></mml:math></inline-formula>, and the value of the unchosen item decreases by the same amount (<xref ref-type="fig" rid="fig4">Figure 4A</xref>). We refer to the updated values as <italic>d-values</italic>, or <inline-formula><mml:math id="inf15"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msub><mml:mi>v</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>d</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula>, where <inline-formula><mml:math id="inf16"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>d</mml:mi></mml:mstyle></mml:math></inline-formula> stands for ‘dynamic’.</p><fig id="fig4" position="float"><label>Figure 4.</label><caption><title>Revaluation algorithm.</title><p>(<bold>A</bold>) Schematic example of the revaluation algorithm applied to one decision. After a choice between items A and B, the value of the chosen item is increased by <inline-formula><mml:math id="inf17"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>δ</mml:mi></mml:mstyle></mml:math></inline-formula> and the value of the unchosen item is decreased by the same amount. (<bold>B</bold>) Example of value changes due to revaluation, for three items, as a function of the presentation number within the session. In the experiment, each item was presented seven times. (<bold>C</bold>) Deviance of the of the logistic regression model fit with the values assigned by the Reval procedure to the data from one participant, for different values of <inline-formula><mml:math id="inf18"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>δ</mml:mi></mml:mstyle></mml:math></inline-formula>. The best fitting value is $0.15. The inset shows a histogram of the best-fitting <inline-formula><mml:math id="inf19"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>δ</mml:mi></mml:mstyle></mml:math></inline-formula> values across participants.</p></caption><graphic mimetype="image" mime-subtype="tiff" xlink:href="elife-96997-fig4-v1.tif"/></fig><p><xref ref-type="fig" rid="fig4">Figure 4B</xref> illustrates how the value of the items changes over the course of the session, for a given value of <inline-formula><mml:math id="inf20"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>δ</mml:mi></mml:mstyle></mml:math></inline-formula>, for three snack items. For example, while the item shown with the green curve is initially very valuable, as indicated by its high initial rating, its value decreases over the course of the session each time it was not selected.</p><p>We determined the degree of revaluation that best explained the participants’ choices. For each participant, we find the value of <inline-formula><mml:math id="inf21"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>δ</mml:mi></mml:mstyle></mml:math></inline-formula> that minimizes the deviance of a logistic regression model that uses the <italic>d-values</italic> to fit the choices made on each trial,<disp-formula id="equ1"><label>(1)</label><mml:math id="m1"><mml:mrow><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mrow><mml:mi mathvariant="normal">l</mml:mi><mml:mi mathvariant="normal">o</mml:mi><mml:mi mathvariant="normal">g</mml:mi><mml:mi mathvariant="normal">i</mml:mi><mml:mi mathvariant="normal">t</mml:mi></mml:mrow><mml:mo stretchy="false">[</mml:mo><mml:msub><mml:mi>p</mml:mi><mml:mrow><mml:mi mathvariant="normal">c</mml:mi><mml:mi mathvariant="normal">h</mml:mi><mml:mi mathvariant="normal">o</mml:mi><mml:mi mathvariant="normal">i</mml:mi><mml:mi mathvariant="normal">c</mml:mi><mml:mi mathvariant="normal">e</mml:mi></mml:mrow></mml:msub><mml:mo stretchy="false">]</mml:mo><mml:mo>=</mml:mo><mml:msub><mml:mi>β</mml:mi><mml:mn>0</mml:mn></mml:msub><mml:mo>+</mml:mo><mml:msub><mml:mi>β</mml:mi><mml:mn>1</mml:mn></mml:msub><mml:msubsup><mml:mi>v</mml:mi><mml:mi>d</mml:mi><mml:mrow><mml:mrow><mml:mo stretchy="false">(</mml:mo><mml:mi mathvariant="normal">l</mml:mi><mml:mi mathvariant="normal">e</mml:mi><mml:mi mathvariant="normal">f</mml:mi><mml:mi mathvariant="normal">t</mml:mi><mml:mo stretchy="false">)</mml:mo></mml:mrow></mml:mrow></mml:msubsup><mml:mo>+</mml:mo><mml:msub><mml:mi>β</mml:mi><mml:mn>2</mml:mn></mml:msub><mml:msubsup><mml:mi>v</mml:mi><mml:mi>d</mml:mi><mml:mrow><mml:mrow><mml:mo stretchy="false">(</mml:mo><mml:mi mathvariant="normal">r</mml:mi><mml:mi mathvariant="normal">i</mml:mi><mml:mi mathvariant="normal">g</mml:mi><mml:mi mathvariant="normal">h</mml:mi><mml:mi mathvariant="normal">t</mml:mi><mml:mo stretchy="false">)</mml:mo></mml:mrow></mml:mrow></mml:msubsup><mml:mo>,</mml:mo></mml:mstyle></mml:mrow></mml:math></disp-formula></p><p>where <inline-formula><mml:math id="inf22"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msub><mml:mi>p</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi mathvariant="normal">c</mml:mi><mml:mi mathvariant="normal">h</mml:mi><mml:mi mathvariant="normal">o</mml:mi><mml:mi mathvariant="normal">i</mml:mi><mml:mi mathvariant="normal">c</mml:mi><mml:mi mathvariant="normal">e</mml:mi></mml:mrow></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula> is the probability of choosing the item that was presented on the right. The <italic>d-values</italic> are initialized to the explicitly reported values for all items, and they are updated by plus or minus <inline-formula><mml:math id="inf23"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>δ</mml:mi></mml:mstyle></mml:math></inline-formula> when an item is chosen or rejected, respectively. Importantly, the updated values only affect future decisions involving the items.</p><p><xref ref-type="fig" rid="fig4">Figure 4C</xref> shows the deviance of the logistic regression model for a representative participant, as a function of <inline-formula><mml:math id="inf24"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>δ</mml:mi></mml:mstyle></mml:math></inline-formula>. For this participant, the best explanation of the choices is obtained with a value of <inline-formula><mml:math id="inf25"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>δ</mml:mi><mml:mo>≈</mml:mo><mml:mi mathvariant="normal">$</mml:mi><mml:mn>0.15</mml:mn></mml:mstyle></mml:math></inline-formula>. We fit the value of <inline-formula><mml:math id="inf26"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>δ</mml:mi></mml:mstyle></mml:math></inline-formula> independently for each participant to minimize the deviance of the logistic regression model fit to the choices. On average, each choice changed the value of the chosen and unchosen items by <inline-formula><mml:math id="inf27"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">$</mml:mi><mml:mn>0.18</mml:mn><mml:mo>±</mml:mo><mml:mn>0.016</mml:mn></mml:mstyle></mml:math></inline-formula> (mean ± s.e.m., (<xref ref-type="fig" rid="fig4">Figure 4C</xref>), <italic>inset</italic>).</p><p>The values derived from the <italic>Reval</italic> algorithm explain the choices better than the explicit value reports. The choices are more sensitive to variation in <inline-formula><mml:math id="inf28"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>d</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula>, evidenced by the steeper slope (<xref ref-type="fig" rid="fig5">Figure 5A</xref>). When <inline-formula><mml:math id="inf29"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>d</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula> and <inline-formula><mml:math id="inf30"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>s</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula> are allowed to compete for the same binomial variance, the former explains away the latter. This assertion is supported by a logistic regression model that incorporates both <inline-formula><mml:math id="inf31"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>s</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula> and <inline-formula><mml:math id="inf32"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>d</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula> as explanatory variables (<xref ref-type="disp-formula" rid="equ7">Equation 7</xref>). The coefficient associated with <inline-formula><mml:math id="inf33"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>s</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula> is not significantly different from zero while the one associated with <inline-formula><mml:math id="inf34"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>d</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula> remains positive and highly significant (<xref ref-type="fig" rid="fig5s1">Figure 5—figure supplement 1</xref>).</p><fig-group><fig id="fig5" position="float"><label>Figure 5.</label><caption><title>Revaluation explains choice and RT better than static values.</title><p>(<bold>A</bold>) Proportion of rightward choices (top) and mean response time (bottom) as function of the difference in <italic>d-value</italic> between the two items. The black lines are fits of a drift-diffusion model that uses the <italic>d-values</italic>. The red lines correspond to the fits of a DDM that uses the <italic>s-values</italic> (same as in <xref ref-type="fig" rid="fig1">Figure 1C–D</xref>). Error bars indicate s.e.m. across trials. Participants are more sensitive to <italic>d-values</italic> than <italic>s-values</italic> (top) and the <italic>d-values</italic> better explain the full range of RTs (bottom). (<bold>B</bold>) Percentage of variance in response times explained by a <italic>DDM</italic> in which the drift rate depends on either <inline-formula><mml:math id="inf35"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mrow><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow><mml:mi>d</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:mrow></mml:mstyle></mml:math></inline-formula> (abscissa) or <inline-formula><mml:math id="inf36"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mrow><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow><mml:mi>s</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:mrow></mml:mstyle></mml:math></inline-formula> (ordinate). Each data point corresponds to a different participant. For most participants, the model based on the dynamic values explained a greater proportion of the variance. (<bold>C</bold>) <italic>d-values</italic> are better than <italic>s-values</italic> at predicting the difficulty of a decision as reflected in the response times. Data points represent the difference in mean RTs between difficult and easy decisions. Positive values indicate that difficult decisions take longer on average than easy ones. <italic>Difficult</italic> and <italic>easy</italic> are defined relative to the median of the absolute value of <inline-formula><mml:math id="inf37"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mrow><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow><mml:mi>s</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:mrow></mml:mstyle></mml:math></inline-formula> (left) or <inline-formula><mml:math id="inf38"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mrow><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow><mml:mi>d</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:mrow></mml:mstyle></mml:math></inline-formula> (right). The lines connect the mean RTs of each participant. P-value is from a paired t-test.</p></caption><graphic mimetype="image" mime-subtype="tiff" xlink:href="elife-96997-fig5-v1.tif"/></fig><fig id="fig5s1" position="float" specific-use="child-fig"><label>Figure 5—figure supplement 1.</label><caption><title>Static and dynamic values competing to explain choice.</title><p>We fit the logistic regression model indicated in the figure separately for each participant, where <inline-formula><mml:math id="inf39"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mi>s</mml:mi></mml:msub></mml:mrow></mml:mstyle></mml:math></inline-formula> and <inline-formula><mml:math id="inf40"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mrow><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow><mml:msub><mml:mrow><mml:mrow><mml:mpadded width="0"><mml:mphantom><mml:mn>10</mml:mn><mml:mi>p</mml:mi><mml:mi>t</mml:mi></mml:mphantom></mml:mpadded></mml:mrow></mml:mrow><mml:mi>d</mml:mi></mml:msub></mml:mrow></mml:msub></mml:mstyle></mml:mrow></mml:mstyle></mml:math></inline-formula> are the difference in static and dynamic values for each trial, respectively. The ordinate show the regression coefficient associated with <inline-formula><mml:math id="inf41"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mrow><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow><mml:mi>s</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:mrow></mml:mstyle></mml:math></inline-formula> and the abscissa show the regression coefficient associated with <inline-formula><mml:math id="inf42"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mrow><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow><mml:mi>d</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:mrow></mml:mstyle></mml:math></inline-formula>. Each data point corresponds to a different participant. Error bars indicate the standard error of the associated regression coefficient.</p></caption><graphic mimetype="image" mime-subtype="tiff" xlink:href="elife-96997-fig5-figsupp1-v1.tif"/></fig><fig id="fig5s2" position="float" specific-use="child-fig"><label>Figure 5—figure supplement 2.</label><caption><title>Comparison of <italic>DDM</italic> fits using static and dynamic values.</title><p>(<bold>A</bold>) BIC comparison between the <italic>DDM</italic> in which the drift rate depends on either <inline-formula><mml:math id="inf43"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mrow><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow><mml:mi>d</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:mrow></mml:mstyle></mml:math></inline-formula> or.<inline-formula><mml:math id="inf44"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mrow><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow><mml:mi>s</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:mrow></mml:mstyle></mml:math></inline-formula> The comparison favors the model that uses the dynamic values for all participants. (<bold>B</bold>) Same as A, but for choice and response time data simulated from the <italic>DDM</italic> fit to the participants’ data using the static (i.e. explicitly reported) values.</p></caption><graphic mimetype="image" mime-subtype="tiff" xlink:href="elife-96997-fig5-figsupp2-v1.tif"/></fig><fig id="fig5s3" position="float" specific-use="child-fig"><label>Figure 5—figure supplement 3.</label><caption><title>Similar <inline-formula><mml:math id="inf45"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>δ</mml:mi></mml:mstyle></mml:math></inline-formula> values obtained by <italic>Reval</italic> and logistic regression.</title><p>Comparison of the <inline-formula><mml:math id="inf46"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>δ</mml:mi></mml:mstyle></mml:math></inline-formula> values obtained by the <italic>Reval</italic> algorithm, and by an alternative approach that uses a single logistic regression model, applied to each participant’s data, that takes into account the number of times the items in the current trial were presented and either chosen or not chosen in previous trials (<xref ref-type="disp-formula" rid="equ14">Equation 14</xref>). Each data point corresponds to one participant. The method lead to values of <inline-formula><mml:math id="inf47"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>δ</mml:mi></mml:mstyle></mml:math></inline-formula> which are almost identical to <italic>Reval</italic>.</p></caption><graphic mimetype="image" mime-subtype="tiff" xlink:href="elife-96997-fig5-figsupp3-v1.tif"/></fig></fig-group><p>More surprisingly, <italic>Reval</italic> allows us to explain the response times better than the explicit value reports, even though RTs were not used to establish the <italic>d-values</italic>. We used the <italic>d-values</italic> to fit a drift-diffusion model to the single-trial choice and response time data, and compared this model with the one that was fit using the <italic>s-values</italic> (<xref ref-type="fig" rid="fig5">Figure 5A</xref>). To calculate the fraction of RT variance explained by each model, we subtracted from each trial’s RT the models’ expectation, conditional on <inline-formula><mml:math id="inf48"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>x</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula> (with <inline-formula><mml:math id="inf49"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mrow><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>x</mml:mi><mml:mo>∈</mml:mo><mml:mo fence="false" stretchy="false">{</mml:mo><mml:mi>s</mml:mi><mml:mo>,</mml:mo><mml:mi>d</mml:mi><mml:mo fence="false" stretchy="false">}</mml:mo></mml:mstyle></mml:mrow></mml:mstyle></mml:math></inline-formula>) and choice. The model that relies on the <italic>d-values</italic> explains a larger fraction of variance in RT than the model that relies on the <italic>s-values</italic> (<xref ref-type="fig" rid="fig5">Figure 5B</xref>). This indicates that the re-assignment of values following <italic>Reval</italic> improved the capacity of a <italic>DDM</italic> to explain the response times.</p><p>The <italic>DDM</italic> that uses the dynamic values also explains the combined choice-RT data better than the one that uses the static values. We compared their goodness of fit using the Bayesian Information Criteria (BIC), penalizing the <italic>DDM</italic> that uses the dynamic values for the revaluation update parameter, <inline-formula><mml:math id="inf50"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>δ</mml:mi></mml:mstyle></mml:math></inline-formula>. For all participants, the <italic>DDM</italic> that uses the dynamic values provided a better fit than the <italic>DDM</italic> that uses the static values (<xref ref-type="fig" rid="fig5s2">Figure 5—figure supplement 2A</xref>). To control for the possibility that the model comparison is biased by the extra parameter in the dynamic model (<inline-formula><mml:math id="inf51"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>δ</mml:mi></mml:mstyle></mml:math></inline-formula>), we simulated choice and RT data for each participant from the <italic>DDM</italic> model fit to the static values, and fit these simulated data to the DDMs using static and dynamic values (in the latter case applying the <italic>Reval</italic> algorithm prior to fitting). For the simulated data, the model comparison favored the <italic>DDM</italic> using static values for most participants (<xref ref-type="fig" rid="fig5s2">Figure 5—figure supplement 2B</xref>), indicating that the additional parameter in the dynamic model does not strongly bias the model comparison.</p><p>The time it takes to make a decision, and the difference in value between the items under comparison, can be considered complementary measures of decision difficulty. On average, the more similar in value the two items are, the longer it would take to commit to a choice. Under this assumption, we can compare how well the static and the dynamic values predict the difficulty of the choices as judged by their response times. The application of <italic>Reval</italic> revealed that some decisions that were initially considered difficult, because <inline-formula><mml:math id="inf52"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>s</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula> was small, were actually easy, because <inline-formula><mml:math id="inf53"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>d</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula> was large, and vice versa. Grouping trials by the <inline-formula><mml:math id="inf54"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>d</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula> led to a wider range of mean RTs compared to when we grouped them by <inline-formula><mml:math id="inf55"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>s</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula> (<xref ref-type="fig" rid="fig5">Figure 5A</xref>). The effect can also be observed for individual participants (<xref ref-type="fig" rid="fig5">Figure 5C</xref>). For each participant, we grouped trials into two categories depending on whether the difference in value was less than or greater than the median difference. We then calculated the mean RT for each of the two groups of trials. The difference in RT between the two groups was greater when we grouped the trials using the <italic>d-values</italic> than when we used the <italic>s-values</italic>. This implies the <italic>d-values</italic> were better than the <italic>s-values</italic> at assessing the difficulty of a decision as reflected in the response time.</p><p>We verified that the improvement in fit was not just due to the additional free parameter (<inline-formula><mml:math id="inf56"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>δ</mml:mi></mml:mstyle></mml:math></inline-formula>). To do this, we again used simulated choices sampled from logistic regression models fit to the participants’ choices, as we did for <xref ref-type="fig" rid="fig2">Figure 2</xref>. Because the choices are sampled from logistic functions fit to the choice data, they lead to a psychometric function that is similar to that obtained with the experimental data. We reasoned that if revaluation were an artifact of the analysis method, then applying the revaluation algorithm to these simulated data should lead to values of <inline-formula><mml:math id="inf57"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>δ</mml:mi></mml:mstyle></mml:math></inline-formula> and goodness of fit similar to those of the real data. To the contrary, (<italic>i</italic>) the optimal values of <inline-formula><mml:math id="inf58"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>δ</mml:mi></mml:mstyle></mml:math></inline-formula> for the simulated data were close to zero (<xref ref-type="fig" rid="fig6">Figure 6A</xref>); (<italic>ii</italic>) the reduction in deviance after applying <italic>Reval</italic> was negligible compared to the reduction in the actual data (<xref ref-type="fig" rid="fig6">Figure 6B</xref>); and (<italic>iii</italic>) we found no significant difference in the RT median splits between <italic>s-values</italic> and <italic>d-values</italic> (<xref ref-type="fig" rid="fig6">Figure 6C</xref>). This shows that the improvements in fit quality due to <italic>Reval</italic> are neither guaranteed nor an artifact of the procedure.</p><fig id="fig6" position="float"><label>Figure 6.</label><caption><title>No revaluation in simulated data.</title><p>(<bold>A</bold>) Histogram of the best-fitting revaluation update (<inline-formula><mml:math id="inf59"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>δ</mml:mi></mml:mstyle></mml:math></inline-formula>) for data simulated by sampling choices from a logistic function fit to the participants’ choices. The best-fitting <inline-formula><mml:math id="inf60"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>δ</mml:mi></mml:mstyle></mml:math></inline-formula> values for the simulated choices are centered around 0. For reference, we have also included a histogram of the <inline-formula><mml:math id="inf61"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>δ</mml:mi></mml:mstyle></mml:math></inline-formula> values obtained from the fits to the participants’ data, showing all positive values (gray). (<bold>B</bold>) Deviance of the logistic regression model used to explain the choices (<xref ref-type="disp-formula" rid="equ1">Equation 1</xref>), fit using either the static values (ordinate) or the <italic>Reval</italic> algorithm (abscissa). Each data point corresponds to a different participant. Experimental data are shown in gray and simulated data (as in panel A) are shown in red. The marked reduction in deviance in the experimental data is absent in the data simulated by sampling from logistic regressions fit to the static values. (<bold>C</bold>) The same analysis shown in <xref ref-type="fig" rid="fig5">Figure 5C</xref>, applied to the simulated data. The values obtained from <italic>Reval</italic> were no better than the static values at explaining the RTs, as expected, since the <inline-formula><mml:math id="inf62"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>δ</mml:mi></mml:mstyle></mml:math></inline-formula> values were ∼0 and thus <inline-formula><mml:math id="inf63"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msub><mml:mi>v</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>d</mml:mi></mml:mrow></mml:msub><mml:mo>≈</mml:mo><mml:msub><mml:mi>v</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>s</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula>. Same conventions as in <xref ref-type="fig" rid="fig5">Figure 5C</xref>.</p></caption><graphic mimetype="image" mime-subtype="tiff" xlink:href="elife-96997-fig6-v1.tif"/></fig></sec><sec id="s2-5"><title>Imperfect value reports do not explain revaluation away</title><p>The idea that a choice can induce a change in preference is certainly not new (<xref ref-type="bibr" rid="bib23">Festinger, 1957</xref>). Choice-induced preference change (CIPC) has been documented using a <italic>free-choice paradigm</italic> (<xref ref-type="bibr" rid="bib11">Brehm, 1956</xref>), whereby participants first rate several items, and then choose between pairs of items to which they have assigned the same rating, and finally rate the items again. A robust finding is that items that were chosen are given higher ratings and items that were not chosen are given lower ratings relative to pre-choice ratings, leading to the interpretation that the act of choosing changes the preferences for the items under comparison. However, it has been suggested that the CIPC demonstrated with the free-choice paradigm can be explained as an artifact (<xref ref-type="bibr" rid="bib16">Chen and Risen, 2010</xref>). Put simply, the initial report of value may be a noisy rendering of the true latent value of the item. If two items, A and B, received the same rating but A was chosen over B, then it is likely that the true value for item A is greater than for item B, not because the act of choosing changes preferences, but because the choices are informative about the true values of the items, which are unchanging.</p><p>We examined whether <italic>Reval</italic> could be explained by the same artifact. We considered the possibility that the items’ valuation in the choice phase are static but potentially different from those reported in the ratings phase. If the values are static, but different from those explicitly reported, then <italic>Reval</italic> could still improve choice and RT predictions by revealing the true subjective value of the items.</p><p>We reasoned that if values were static, the improvements we observed in the logistic fits when we applied <italic>Reval</italic> should be the same regardless of how we ordered the trials before applying it. To test this, we applied <italic>Reval</italic> in the order in which the trials were presented in the experiment, and also in the reverse order (i.e. from the last trial to the first). If the values were static, then the quality of the fits should be statistically identical in both cases. In contrast, we observed that the variance explained by <italic>Reval</italic> was greater (i.e. the deviance was lower) when it was applied in the correct order than when it was applied in the opposite order (<xref ref-type="fig" rid="fig7">Figure 7A</xref>; p&lt;0.0001, paired t-test). This rules out the possibility that the values were static. Moreover, the values produced by applying <italic>Reval</italic> in the reverse direction explained the choices better than the static values (<xref ref-type="fig" rid="fig7">Figure 7B</xref>). This might seem counterintuitive, given that the initial values for the <italic>Reval</italic> algorithm are the <italic>s-values</italic>, which are explicitly reported <italic>before</italic> the main experiment. In a later section, we show that this effect stems from the same process that gives rise to revaluation (Is revaluation a byproduct of deliberation?).</p><fig id="fig7" position="float"><label>Figure 7.</label><caption><title><italic>Reval</italic> is sensitive to trial order.</title><p>(<bold>A</bold>) Deviance obtained by applying <italic>Reval</italic> to the trials in the order in which they were completed (abscissa) and in the reverse order (ordinate). Each data point corresponds to a different participant. The deviance is greater (i.e. the fits are worse) when <italic>Reval</italic> is applied in the reverse direction. (<bold>B</bold>) The deviance of the logistic regression model used to explain the choices (<xref ref-type="disp-formula" rid="equ1">Equation 1</xref>), obtained by applying <italic>Reval</italic> in the backward direction (ordinate), is lower (i.e. the fits are better) than the deviance obtained using the static values (abscissa). Each data point corresponds to a different participant.</p></caption><graphic mimetype="image" mime-subtype="tiff" xlink:href="elife-96997-fig7-v1.tif"/></fig></sec><sec id="s2-6"><title>Asymmetric value-updating for chosen and unchosen options</title><p>So far we have assumed that a choice increases the value of the chosen option by <inline-formula><mml:math id="inf64"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>δ</mml:mi></mml:mstyle></mml:math></inline-formula> and decreases the value of the unchosen option by the same amount. Here, we evaluate the possibility that the degree of revaluation is different for the chosen and unchosen options. We fit a variant of the <italic>Reval</italic> algorithm with two values of <inline-formula><mml:math id="inf65"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>δ</mml:mi></mml:mstyle></mml:math></inline-formula>, one for the chosen option (<inline-formula><mml:math id="inf66"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msub><mml:mi>δ</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi mathvariant="normal">c</mml:mi><mml:mi mathvariant="normal">h</mml:mi><mml:mi mathvariant="normal">o</mml:mi><mml:mi mathvariant="normal">s</mml:mi><mml:mi mathvariant="normal">e</mml:mi><mml:mi mathvariant="normal">n</mml:mi></mml:mrow></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula>) and one for the unchosen option (<inline-formula><mml:math id="inf67"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msub><mml:mi>δ</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi mathvariant="normal">u</mml:mi><mml:mi mathvariant="normal">n</mml:mi><mml:mi mathvariant="normal">c</mml:mi><mml:mi mathvariant="normal">h</mml:mi><mml:mi mathvariant="normal">o</mml:mi><mml:mi mathvariant="normal">s</mml:mi><mml:mi mathvariant="normal">e</mml:mi><mml:mi mathvariant="normal">n</mml:mi></mml:mrow></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula>). <xref ref-type="fig" rid="fig8">Figure 8</xref> shows the values that best fit the data for each participant. For each participant, <inline-formula><mml:math id="inf68"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msub><mml:mi>δ</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi mathvariant="normal">c</mml:mi><mml:mi mathvariant="normal">h</mml:mi><mml:mi mathvariant="normal">o</mml:mi><mml:mi mathvariant="normal">s</mml:mi><mml:mi mathvariant="normal">e</mml:mi><mml:mi mathvariant="normal">n</mml:mi></mml:mrow></mml:mrow></mml:msub><mml:mrow class="MJX-TeXAtom-ORD"><mml:mo>&gt;</mml:mo></mml:mrow><mml:mn>0</mml:mn></mml:mstyle></mml:math></inline-formula> and <inline-formula><mml:math id="inf69"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msub><mml:mi>δ</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi mathvariant="normal">u</mml:mi><mml:mi mathvariant="normal">n</mml:mi><mml:mi mathvariant="normal">c</mml:mi><mml:mi mathvariant="normal">h</mml:mi><mml:mi mathvariant="normal">o</mml:mi><mml:mi mathvariant="normal">s</mml:mi><mml:mi mathvariant="normal">e</mml:mi><mml:mi mathvariant="normal">n</mml:mi></mml:mrow></mml:mrow></mml:msub><mml:mrow class="MJX-TeXAtom-ORD"><mml:mo>&lt;</mml:mo></mml:mrow><mml:mn>0</mml:mn></mml:mstyle></mml:math></inline-formula>; in other words, the value of the chosen item typically increases, while the value of the unchosen item tends to decrease following a choice. Further, for most participants, the degree of revaluation is greater for the chosen option than for the unchosen option. As we speculate in the discussion, this result may be related to the unequal distribution of attention between the chosen and unchosen items (<xref ref-type="bibr" rid="bib44">Krajbich et al., 2010</xref>).</p><fig id="fig8" position="float"><label>Figure 8.</label><caption><title>Stronger revaluation for the chosen than for the unchosen item.</title><p>We fit a variant of the <italic>Reval</italic> algorithm that includes separate update values (<inline-formula><mml:math id="inf70"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>δ</mml:mi></mml:mstyle></mml:math></inline-formula>) for the chosen and unchosen options. The best-fitting <inline-formula><mml:math id="inf71"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>δ</mml:mi></mml:mstyle></mml:math></inline-formula> value for the chosen option (abscissa) is plotted against the best-fitting value for the unchosen option (ordinate). Each data point corresponds to one participant. The increase in value for the chosen option is greater than the decrease in value for the unchosen option (paired t-test).</p></caption><graphic mimetype="image" mime-subtype="tiff" xlink:href="elife-96997-fig8-v1.tif"/></fig></sec><sec id="s2-7"><title>Representation of revalued values in the ventromedial prefrontal cortex</title><p>Several brain areas, in particular the ventromedial prefrontal cortex (vmPFC), have been shown to represent the value of decision alternatives during value-based decisions (<xref ref-type="bibr" rid="bib40">Kennerley et al., 2009</xref>; <xref ref-type="bibr" rid="bib55">Plassmann et al., 2007</xref>; <xref ref-type="bibr" rid="bib6">Bartra et al., 2013</xref>). Based on our finding that the <italic>d-values</italic> provide a better explanation of the behavioral data than the <italic>s-values</italic>, we reasoned that the <italic>d-values</italic> might explain the BOLD activity in these areas beyond that explained by the <italic>s-values</italic>. We included both the <italic>s-value</italic> and the <italic>d-value</italic> of the chosen item in a whole-brain regression analysis of BOLD activity. This parameterization reveals significant correlation of the BOLD signal in the vmPFC with <italic>d-value</italic>, controlling for <italic>s-value</italic> (<xref ref-type="fig" rid="fig9">Figure 9</xref> and <xref ref-type="supplementary-material" rid="supp1">Supplementary file 1</xref>). In fact, in a separate model that only included <italic>s-value</italic>, the effect of <italic>s-value</italic> on BOLD in the vmPFC did not survive correction for familywise error rate at a whole-brain level (<xref ref-type="fig" rid="fig9s1">Figure 9—figure supplement 1b</xref> and <xref ref-type="supplementary-material" rid="supp2">Supplementary file 2</xref> top). In contrast, another model that only included <italic>d-value</italic> revealed a robust effect of <italic>d-value</italic> on BOLD in vmPFC that survived whole-brain correction (<xref ref-type="fig" rid="fig9s1">Figure 9—figure supplement 1</xref> and <xref ref-type="supplementary-material" rid="supp2">Supplementary file 2</xref> middle). Finally, to evaluate whether the effect shown in <xref ref-type="fig" rid="fig9">Figure 9</xref> is not simply captured by the difference in <italic>d-value</italic> and <italic>s-value</italic>, we ran a fourth model that included only (<italic>d-value</italic><inline-formula><mml:math id="inf72"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mo>−</mml:mo></mml:mstyle></mml:math></inline-formula><italic>s-value</italic>). The effect of this difference between <italic>d-value</italic> and <italic>s-value</italic> on BOLD in vmPFC did not survive whole-brain correction (<xref ref-type="fig" rid="fig9s1">Figure 9—figure supplement 1</xref> and <xref ref-type="supplementary-material" rid="supp2">Supplementary file 2</xref> bottom). Collectively, these findings provide additional evidence for revaluation, as capturing a meaningful aspect of the data, in the sense that it accounts for the activity of brain areas known to reflect the value of the choice alternatives.</p><fig-group><fig id="fig9" position="float"><label>Figure 9.</label><caption><title>Revaluation reflected in BOLD activity in ventromedial prefrontal cortex.</title><p>Brain-wide fMRI analysis revealed a significant correlation between <italic>d-values</italic> and activity in the vmPFC, after controlling for <italic>s-values</italic>. The statistical map was projected onto the cortical surface. Shown here are the medial views of the right and left hemispheres of a semi-inflated surface of a template brain. Heatmap color bars range from z-stat=3.1–3.6. The map was cluster corrected for familywise error rate at a whole-brain level with an uncorrected cluster-forming threshold of z=3.1 and corrected extent of <italic>P</italic>&lt;0.05. The full unthresholded map can be viewed here: <ext-link ext-link-type="uri" xlink:href="https://identifiers.org/neurovault.image:869963">https://identifiers.org/neurovault.image:869963</ext-link>.</p></caption><graphic mimetype="image" mime-subtype="tiff" xlink:href="elife-96997-fig9-v1.tif"/></fig><fig id="fig9s1" position="float" specific-use="child-fig"><label>Figure 9—figure supplement 1.</label><caption><title><italic>d-value</italic>, but to a lesser extent <italic>s-value</italic> and the difference between the two, is reflected in BOLD activity in ventromedial prefrontal cortex.</title><p>Brain-wide fMRI analyses with whole-brain correction for multiple comparisons revealed (1) no significant correlation between <italic>s-value</italic> and activity in the vmPFC, but a significant correlation with BOLD in the striatum and in the precuneus when only <italic>s-value</italic> was included in the model (top), (2) a significant correlation between <italic>d-value</italic> and BOLD in vmPFC, striatum, and precuneus in a model that only included <italic>d-value</italic> (middle), and (3) no significant correlation between the difference between <italic>d-value</italic> and <italic>s-value</italic> in the vmPFC when only this difference is included in the model. The statistical maps from these three independent models were projected onto the cortical surface. Shown here are the medial view of the right and left hemispheres of a semi-inflated surface of a template brain. The heatmap color bar ranges from z-stat=3.1–3.6. All maps were cluster corrected for familywise error rate at a whole-brain level with an uncorrected cluster-forming threshold of z=3.1 and corrected extent of p&lt;0.05. Full unthresholded maps can be viewed here: <ext-link ext-link-type="uri" xlink:href="https://identifiers.org/neurovault.collection:17498">https://identifiers.org/neurovault.collection:17498</ext-link>.</p></caption><graphic mimetype="image" mime-subtype="tiff" xlink:href="elife-96997-fig9-figsupp1-v1.tif"/></fig></fig-group></sec><sec id="s2-8"><title>Revaluation in other datasets of the food-choice task</title><p>To assess the generality of our behavioral results, we applied <italic>Reval</italic> to other publicly available datasets. All involve binary choices between food snacks, similar to <xref ref-type="bibr" rid="bib5">Bakkour et al., 2019</xref>. We analyze data from experiments reported in <xref ref-type="bibr" rid="bib24">Folke et al., 2016</xref> and from the two value-based decision tasks reported in <xref ref-type="bibr" rid="bib63">Sepulveda et al., 2020</xref>.</p><p><italic>Reval</italic> yields results that are largely similar to those observed in the data from <xref ref-type="bibr" rid="bib5">Bakkour et al., 2019</xref>. The values derived from <italic>Reval</italic> led to a better classification of choice difficulty than the explicit value reports (<xref ref-type="fig" rid="fig10">Figure 10A</xref>). In all three datasets, the <inline-formula><mml:math id="inf73"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>δ</mml:mi></mml:mstyle></mml:math></inline-formula> values were significantly larger than those obtained from simulated data under the assumption that the values were static and equal to the explicitly reported values (<xref ref-type="fig" rid="fig10">Figure 10B</xref>). Furthermore, the reduction in the deviance resulting from the application of <italic>Reval</italic> (<xref ref-type="disp-formula" rid="equ7">Equation 7</xref>) was significantly greater than the reduction observed in simulated data (<xref ref-type="fig" rid="fig10">Figure 10C</xref>). [All p-values, derived from two-tailed paired t-tests, are shown in the figure].</p><fig id="fig10" position="float"><label>Figure 10.</label><caption><title>Revaluation observed in other datasets.</title><p>We applied the <italic>Reval</italic> method to other publicly available datasets of the food choice task. In the experiment of <xref ref-type="bibr" rid="bib24">Folke et al., 2016</xref> (first column), participants reported their willingness to pay for each of 16 common snack items. In the choice task, they were presented with each unique pair of items and asked to choose the preferred item. Each unique pair was presented twice for a total of 240 trials per participant. In the experiment of <xref ref-type="bibr" rid="bib63">Sepulveda et al., 2020</xref> (second and third columns), participants (N=31) reported their willingness to pay for each of 60 snack items. They were then presented with pairs of items from which to choose. Pairs were selected based on participants’ willingness-to-pay reports to provide comparisons between pairs of high-value, low-value and mixed-value items. The choice task was performed under two framing conditions: <italic>like-framing</italic>, selecting the more preferred item, and <italic>dislike framing</italic>, selecting the less preferred item. The task consisted of six alternating blocks of <italic>like-</italic> and <italic>dislike-framing</italic> (40 trials per block). (<bold>A</bold>) RT difference between <italic>easy</italic> and <italic>difficult</italic> trials, determined as a median split of <inline-formula><mml:math id="inf74"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mrow class="MJX-TeXAtom-ORD"><mml:mo stretchy="false">|</mml:mo></mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:mi>v</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mo stretchy="false">|</mml:mo></mml:mrow></mml:mstyle></mml:math></inline-formula>. Same analysis as in <xref ref-type="fig" rid="fig5">Figure 5C</xref>. (<bold>B</bold>) Histogram of the best-fitting revaluation update (<inline-formula><mml:math id="inf75"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>δ</mml:mi></mml:mstyle></mml:math></inline-formula>) for data simulated by sampling choices from a logistic function fit to the participant’s choices (red), and for the actual data (gray). Same analysis as in <xref ref-type="fig" rid="fig6">Figure 6A</xref>. (<bold>C</bold>) Comparison of the deviance with and without <italic>Reval</italic>. Same analysis as in <xref ref-type="fig" rid="fig6">Figure 6B</xref>. (<bold>D</bold>) Comparison of the deviance applying <italic>Reval</italic> in the forward and backward directions. Same analysis as in <xref ref-type="fig" rid="fig7">Figure 7A</xref>. All p-values shown in the figure are from paired t-tests.</p></caption><graphic mimetype="image" mime-subtype="tiff" xlink:href="elife-96997-fig10-v1.tif"/></fig><p>In the dataset from <xref ref-type="bibr" rid="bib24">Folke et al., 2016</xref>, the deviance was significantly smaller when <italic>Reval</italic> was applied in the forward than in the backward direction, replicating the result in our main experiment. However, in the dataset of <xref ref-type="bibr" rid="bib63">Sepulveda et al., 2020</xref>, no significant difference in deviance was observed (<xref ref-type="fig" rid="fig10">Figure 10D</xref>). We do not know what explains this discrepancy, although we believe that the differences in experimental design may play a role. In the experiment of <xref ref-type="bibr" rid="bib63">Sepulveda et al., 2020</xref>, unlike the other two datasets that we analyzed, participants performed the experiment in two framing conditions: one in which they chose the item the liked the most, and another one in which the chose the item they disliked the most. These two conditions alternated in short blocks of 40 trials. This alternation may affect valuation in a way that is not captured by the <italic>Reval</italic> algorithm. We expand on this in Discussion.</p></sec><sec id="s2-9"><title>Is revaluation a byproduct of deliberation?</title><p>We hypothesize that the sequential dependencies we identified with <italic>Reval</italic> may be a corollary of the process by which values are constructed during deliberation. The subjective value of an item depends on the decision-maker’s <italic>mindset</italic>, which may change more slowly than the rate of trial presentations. Therefore, the subjective value of an item on a given trial may be informative about the value of the item the next time it is presented. Subjective values are not directly observable, but choices are informative about the items’ value.</p><p>We assessed the plausibility of this hypothesis with a bounded evidence accumulation model that includes a parameter that controls the correlation between successive evidence samples for a given item. We call this the <italic>correlated-evidence drift-diffusion model</italic> (<italic>ceDDM</italic>). We assume that the decision is resolved by accumulating evidence for and against the different alternatives until a decision threshold is crossed.</p><p>The model differs from standard drift-diffusion, where the momentary evidence is a sample drawn from a Normal distribution with expectation equal to <inline-formula><mml:math id="inf76"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>s</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula> plus unbiased noise, <inline-formula><mml:math id="inf77"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi class="MJX-tex-caligraphic" mathvariant="script">N</mml:mi></mml:mrow><mml:mo stretchy="false">(</mml:mo><mml:mn>0</mml:mn><mml:mo>,</mml:mo><mml:msqrt><mml:mi>d</mml:mi><mml:mi>t</mml:mi></mml:msqrt><mml:mo stretchy="false">)</mml:mo></mml:mstyle></mml:math></inline-formula>. Instead, the value of each of the items evolves separately such that the expectations of its value updates are constructed as a Markov chain Monte Carlo (MCMC) process thereby introducing autocorrelation between successive samples of the unbiased noise (see Methods). Crucially, the correlation is not limited to the duration of a trial but extends across trials containing the same item. When an item is repeated in another trial, the process continues to evolve from its value at the time a decision was last made for or against the item.</p><p>We fit the model to the data from <xref ref-type="bibr" rid="bib5">Bakkour et al., 2019</xref>. The model was able to capture the relationship between choice, response time and <inline-formula><mml:math id="inf78"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>s</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula> (<xref ref-type="fig" rid="fig11">Figure 11A</xref>). <xref ref-type="fig" rid="fig11">Figure 11B</xref> shows the degree of correlation in the evidence stream as a function of time, for the model that best fit each participant’s data. After 1 s of evidence sampling, the correlation was 0.1062 ± 0.0113 (mean ± s.e.m. across participants). This is neither negligible (which would make the model equivalent to the DDM) nor very high (which would render sequential sampling useless, since it can only average out the noise that is not shared across time).</p><fig id="fig11" position="float"><label>Figure 11.</label><caption><title>Revaluation occurs in a DDM with temporally-correlated noise.</title><p>A drift-diffusion model with non-independent noise (<italic>ceDDM</italic>) captures the main features of revaluation. (<bold>A</bold>) The <italic>ceDDM</italic> accounts for choices (top) and response times (bottom), plotted as a function of the difference in values obtained from explicit reports (<inline-formula><mml:math id="inf79"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>s</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula>). Same data as in <xref ref-type="fig" rid="fig1">Figure 1C–D</xref>. Red curves are simulations of the best-fitting model. Each trial was simulated 100 times. Simulations were first averaged within trials and then averaged across trials. Error bars and bands indicate s.e.m. across trials. (<bold>B</bold>) Noise correlations as a function of time lag, obtained from the best-fitting model. Each curve corresponds to a different participant. (<bold>C</bold>) <inline-formula><mml:math id="inf80"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>δ</mml:mi></mml:mstyle></mml:math></inline-formula> parameters derived by applying <italic>Reval</italic> to simulated data from the best fitting <italic>ceDDM</italic> model to each participant’s data. As in the data, <inline-formula><mml:math id="inf81"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>δ</mml:mi><mml:mo>&gt;</mml:mo><mml:mn>0</mml:mn></mml:mstyle></mml:math></inline-formula> for all participants. (<bold>D</bold>) Similar analysis as in <xref ref-type="fig" rid="fig5">Figure 5C</xref> applied to simulations of the <italic>ceDDM</italic>. As for the data, <italic>Reval</italic> increased the range of RTs obtained after grouping trials by difficulty (by <italic>s-values</italic> on the left and <italic>d-values</italic> on the right; p-value from paired t-test). (<bold>E</bold>) Similar analysis to that of <xref ref-type="fig" rid="fig7">Figure 7A</xref>, using the simulated data. As observed in the data, the deviance resulting from applying <italic>Reval</italic> in the correct trial order (abscissa) is smaller than when applied in the opposite order (p-value from paired t-test). (<bold>F</bold>) Similar analysis to that of <xref ref-type="fig" rid="fig7">Figure 7B</xref>, using the simulated data.</p></caption><graphic mimetype="image" mime-subtype="tiff" xlink:href="elife-96997-fig11-v1.tif"/></fig><p>The assumptions embodied by the <italic>ceDDM</italic> are consistent with the results of the <italic>Reval</italic> analysis. We applied the <italic>Reval</italic> algorithm to simulated data obtained from the best-fitting <italic>ceDDM</italic>. The results were in good agreement with the experimental data. The best-fitting <inline-formula><mml:math id="inf82"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>δ</mml:mi></mml:mstyle></mml:math></inline-formula> values were positive for all participants and in a range similar to what we observed in the data (<xref ref-type="fig" rid="fig11">Figure 11C</xref>). <italic>Reval</italic> increased the range of RTs when trials were divided by difficulty, implying that <italic>Reval</italic> led to a better classification of easy and difficult decisions (<xref ref-type="fig" rid="fig11">Figure 11D</xref>). <italic>Reval</italic> applied to the trials in the true order explained the simulated choices better than when applied in the opposite direction (<xref ref-type="fig" rid="fig11">Figure 11E</xref>). This is because the model assumes that when an item first appears, the last sample obtained for that item was the value reported in the ratings phase for that item. As more samples are obtained for a given item, the correlation with the static values gradually decreases. Additionally, the values obtained from applying <italic>Reval</italic> in the backward direction provided a better explanation of the simulated choices than the static values (<xref ref-type="fig" rid="fig11">Figure 11F</xref>), mirroring the pattern observed observed in the behavioral data (<xref ref-type="fig" rid="fig7">Figure 7B</xref>). Taken together, the success of <italic>ceDDM</italic> implies that the sequential dependencies we identify with <italic>Reval</italic> may be the result of a value construction process necessary to make a preferential choice.</p></sec></sec><sec id="s3" sec-type="discussion"><title>Discussion</title><sec id="s3-1"><title>Sequential dependencies and choice-induced preference change</title><p>We identified sequential dependencies between choices in a value-based decision task. Participants performed a task in which they had to make a sequence of choices among a limited set of items. The best explanation for future choices was obtained by assuming that the subjective value of the chosen item increases and the value of the unchosen item decreases after each decision. Evidence for revaluation was obtained by analyzing the probability that participants make the same decision in pairs of trials with identical options. We also identified revaluation using an algorithm we call <italic>Reval</italic>. The same algorithm allowed us to identify revaluation in other datasets obtained with the food-choice task (<xref ref-type="bibr" rid="bib24">Folke et al., 2016</xref>; <xref ref-type="bibr" rid="bib63">Sepulveda et al., 2020</xref>).</p><p>The sequential effects we identified can be interpreted as a manifestation of choice-induced preference change. The usual paradigms for detecting the presence of CIPCs are based on the comparison of value ratings reported before and after a choice (for a review see <xref ref-type="bibr" rid="bib32">Izuma and Murayama, 2013</xref>; <xref ref-type="bibr" rid="bib20">Enisman et al., 2021</xref>). After a difficult decision, the rating of the chosen alternative often increases and that of the rejected alternative often decreases—an effect termed the ‘spreading of alternatives’. Many variants of the free choice paradigm have been developed to control for or eliminate the statistical artifact reported by <xref ref-type="bibr" rid="bib16">Chen and Risen, 2010</xref>. One common approach is to compare the ‘spreading of alternatives” observed in the free-choice paradigm (rate-choose-rate, or RCR) with a control task in which a different set of participants rate the items twice before the choice phase (RRC). Any spread observed in the RRC condition cannot be explained by the CIPC, since in the RRC condition there is no choice between the two rating phases. The CIPC is measured indirectly, as the difference in the spread of the alternatives between the RCR and the RRC. Other approaches involve asking participants to rate an item that they are led to believe they have chosen, when in fact they have not (<xref ref-type="bibr" rid="bib65">Sharot et al., 2010</xref>; <xref ref-type="bibr" rid="bib36">Johansson et al., 2014</xref>). Any change in ratings cannot be due to the information provided by a choice, since no real choice was made. In addition to the complications introduced by deceiving the participants (e.g. participants may suspect the deception but not mention it to the experimenter), the elimination of a real choice prevents these paradigms from being used to study the process through which subjective values undergo revision during decision formation.</p><p>In contrast, our approach to identify changes in value does not require pre- and post-choice ratings. Instead, it requires a sequence of trials in which the same items are presented multiple times (as in <xref ref-type="bibr" rid="bib51">Luettgau et al., 2020</xref>). The revaluation effect we find cannot be explained by the artifact identified by <xref ref-type="bibr" rid="bib16">Chen and Risen, 2010</xref>. Using trials with identical items, we show that the nearer in time the trials with identical items are to each other, the more likely people are to choose the same option. Further, the revaluation algorithm explains choices better when applied in the order in which the trials were presented than when applied in the reverse order. These observations are inconsistent with the notion that item values are fixed (i.e. do not change) during the experiment, regardless of whether values are the same or different from those reported during the rating phase.</p></sec><sec id="s3-2"><title>Revaluation during or after deliberation?</title><p>We cannot determine with certainty whether the revaluation occurs after the decision or during the deliberation process leading up to the decision. At face value, it might seem that <italic>Reval</italic> implements change after each decision (<xref ref-type="bibr" rid="bib23">Festinger, 1957</xref>). Yet, <italic>Reval</italic> simply identifies a change in value, which may well occur during the deliberation leading to the decision, perhaps owing to a comparison of other items (on other trials) that happen to suggest a dimension of comparison that increases in importance on the current trial (<xref ref-type="bibr" rid="bib46">Lee and Daunizeau, 2020</xref>; <xref ref-type="bibr" rid="bib50">Lichtenstein and Slovic, 2006</xref>). More broadly, the subjective value of an option depends on the <italic>mindset</italic> of the decision maker. This internal state, which in the food-choice task includes aspects such as degree of satiety or sugar craving, can vary over time, causing the value of the items to vary as well. If changes in <italic>mindset</italic> are slow—that is, lasting longer than the duration of a decision—then the value of items will be correlated over time.</p><p>We proposed a decision model (<italic>ceDDM</italic>) in which evidence samples are correlated over time. Fitting the model to account for each participant’s choices and response times produces a revaluation of magnitude similar to what we observed experimentally. It also predicts that applying <italic>Reval</italic> in the direction in which the trials were presented explains the choices better than applying it in the opposite direction, as we observed in the data. This modeling exercise suggests that the CIPC-like effects we identified may be due to processes that occur during the deliberation leading up to a choice, rather than post-decision processes that attempt to reduce cognitive dissonance. To be clear, we interpret the <italic>ceDDM</italic> only as a proxy for a variety of more nuanced processes. If the <italic>mindset</italic> endures many individual decisions, the subjective value of an item will be correlated over time. While the <italic>ceDDM</italic> captures only a small aspect of this complex process, it has allowed us to explain the sequential dependencies we identified with <italic>Reval</italic>.</p><p>The <italic>ceDDM</italic> belongs to a class of sequential sampling models in which the drift rate varies over time. Such models have already been studied in the context of value-based decisions. For example, in the attentional drift-diffusion model (<xref ref-type="bibr" rid="bib44">Krajbich et al., 2010</xref>), the drift rate varies depending on which item is attended, as if the value of the unattended items are discounted by a multiplicative factor. In Dynamic Field Theory (<xref ref-type="bibr" rid="bib13">Busemeyer and Townsend, 1993</xref>), the drift rate varies depending on which attribute is attended. Recently, <xref ref-type="bibr" rid="bib47">Lee and Pezzulo, 2022</xref> showed that a sequential sampling model in which the drift rate varies over time can explain the ‘spreading of alternatives’ (SoA) characteristic of choice-induced preference change. <xref ref-type="bibr" rid="bib47">Lee and Pezzulo, 2022</xref> propose that the initial rating of the items may be constructed using only the most salient attributes of each item, while in a difficult decision more attributes may be considered, leading to a revaluation that informs the rating reported after the decision phase (see also <xref ref-type="bibr" rid="bib74">Voigt et al., 2019</xref>). Consistent with our proposal, <xref ref-type="bibr" rid="bib47">Lee and Pezzulo, 2022</xref> argue that thinking about non-prominent features during decision-making increases the likelihood that these features will be recalled when evaluating options in subsequent instances.</p></sec><sec id="s3-3"><title>More revaluation for the chosen than the unchosen item</title><p>We observed that the degree of revaluation was higher for the chosen item than for the unchosen item. This was revealed by a variant of the <italic>Reval</italic> algorithm in which we allowed both items to have different updates. We speculate that this difference can be explained by the asymmetric distribution of attention between the chosen and unchosen items. It is known that the chosen item is looked at longer than the unchosen item (<xref ref-type="bibr" rid="bib44">Krajbich et al., 2010</xref>). Further, CIPC is more likely for items that are remembered to have been chosen or unchosen (<xref ref-type="bibr" rid="bib60">Salti et al., 2014</xref>). So one possibility is that the revaluation is larger for the chosen than for the unchosen item because participants spent more time looking at the chosen item and thus are more likely to remember it, leading to a larger change in value (<xref ref-type="bibr" rid="bib74">Voigt et al., 2019</xref>).</p><p>Another possibility derives from the constructive view of preferences and the potential role of attention in decision-making. It is often assumed that value-based decisions involve gathering evidence from different alternatives, and that more evidence is gathered from alternatives that are attended to for longer (<xref ref-type="bibr" rid="bib14">Callaway et al., 2021</xref>; <xref ref-type="bibr" rid="bib49">Li and Ma, 2021</xref>; <xref ref-type="bibr" rid="bib44">Krajbich et al., 2010</xref>). In the <italic>ceDDM</italic>, the correlation in value for a given item decreases with the number of evidence samples collected from the item (<xref ref-type="fig" rid="fig11">Figure 11B</xref>). Therefore, the more that attention is focused on a given item, the greater the difference between the item’s value before and after the decision. Because chosen items are attended to for longer than unchosen items (e.g. <xref ref-type="bibr" rid="bib44">Krajbich et al., 2010</xref>), the chosen item should exhibit larger revaluation than the unchosen one, which is what we observed in the data (<xref ref-type="fig" rid="fig8">Figure 8</xref>).</p></sec><sec id="s3-4"><title>Limitations of our study</title><p>One limitation of our study is that we only examined tasks in which static values were elicited from explicit reports of the value of food items. It remains to be determined if other ways of eliciting subjective values (e.g. <xref ref-type="bibr" rid="bib35">Jensen and Miller, 2010</xref>) would lead to similar results. We think so, as the analysis of trials with identical item pairs (<xref ref-type="fig" rid="fig3">Figure 3</xref>) and the difference between forward and backward <italic>Reval</italic> (<xref ref-type="fig" rid="fig7">Figure 7A</xref>) are inconsistent with the notion that values are static, regardless of their precise value. It also remains to be determined if our results will generalize to non-food items whose value is less sensitive to satiety and other dynamic bodily states. Perceptual decisions also exhibit sequential dependencies, and it remains to be explored whether these can be explained as a process of value construction, similar to what we propose here for the food-choice task (<xref ref-type="bibr" rid="bib30">Gupta et al., 2024</xref>; <xref ref-type="bibr" rid="bib18">Cho et al., 2002</xref>; <xref ref-type="bibr" rid="bib79">Zylberberg et al., 2018</xref>; <xref ref-type="bibr" rid="bib2">Abrahamyan et al., 2016</xref>).</p><p>Another limitation of our study is that, in one of the datasets we analyzed (<xref ref-type="bibr" rid="bib63">Sepulveda et al., 2020</xref>), applying <italic>Reval</italic> in the forward direction was no better than applying it in the backward direction (<xref ref-type="fig" rid="fig10">Figure 10</xref>). We speculate that this failure is related to idiosyncrasies of the experimental design, in particular, the use of alternating blocks of trials with different instructions (select preferred vs. select non-preferred). More importantly, <italic>Reval</italic> applied in the backward direction led to a significant reduction in deviance relative to that obtained using the static values (<xref ref-type="fig" rid="fig7">Figure 7B</xref>). This reduction was also observed in the <italic>ceDDM</italic>, suggesting that the effect may be explained by changes in valuation during deliberation. However, we cannot discard a contribution from other, non-dynamic changes in valuation between the rating and choice phase including contextual effects (<xref ref-type="bibr" rid="bib50">Lichtenstein and Slovic, 2006</xref>), stochastic variability in explicit value reporting (<xref ref-type="bibr" rid="bib56">Polanía et al., 2019</xref>), and the limited range of numerical scales used to report value.</p><p>Finally, we emphasize that the <italic>ceDDM</italic> should be interpreted as a proof-of-principle model used to illustrate how stochastic fluctuations in item desirability can explain many of our results. We chose to model value changes following an MCMC process. However, other stochastic processes or other ways of introducing sequential dependencies (e.g. variability in the starting point of evidence accumulation) may also explain the behavioral observations. Furthermore, there likely are other ways to induce changes in the value of items other than through past decisions. For example, attentional manipulations or other experiences (e.g. actual food consumption) may change one’s preference for an item. The current version of the <italic>ceDDM</italic> does not allow for these influences on value, but we see no fundamental limitation to incorporating them in future instantiations of the model.</p></sec><sec id="s3-5"><title>Concluding remarks</title><p>Our research contributes to a growing body of work exploring the impact of memory on decision-making and preference formation (<xref ref-type="bibr" rid="bib9">Biderman et al., 2020</xref>), and in particular to the CIPC. It has been suggested that the retrieval of an item’s value during decision-making renders it susceptible to modification, leading to a revaluation that influences subsequent valuations through a process that has a neural correlate in the hippocampus (<xref ref-type="bibr" rid="bib51">Luettgau et al., 2020</xref>). The link between memorability and preference is also supported by experiments in which the presentation of an item coincides with an unrelated rapid motor response that increases subsequent preference for the item (<xref ref-type="bibr" rid="bib10">Botvinik-Nezer et al., 2021</xref>) and by experiments demonstrating that people prefer items to which they have previously been exposed (<xref ref-type="bibr" rid="bib77">Zajonc, 1968</xref>). As in these studies, ours also highlights the role of memory in revaluation. Due to the associative nature of memory, successive evidence samples are likely to be dependent (<xref ref-type="bibr" rid="bib59">Rhodes and Turvey, 2007</xref>). A compelling illustration of this effect was provided by Elias Costa and colleagues (<xref ref-type="bibr" rid="bib19">Costa et al., 2009</xref>). Participants were asked to report the first word that came to mind when presented with a word generated by another participant, which was then shown to yet another participant. The resulting chain resembled Lévy flights in semantic space, characterized by mostly short transitions to nearby words and occasional large jumps. Similar dynamic processes have been used to describe eye movements during visual search (<xref ref-type="bibr" rid="bib8">Bella-Fernández et al., 2022</xref>) and the movement of animals during reward foraging (<xref ref-type="bibr" rid="bib12">Brown et al., 2007</xref>; <xref ref-type="bibr" rid="bib31">Hills et al., 2015</xref>). It is intriguing to consider that a similar process may describe how decision-makers search their memory for evidence that bears on a decision.</p></sec></sec><sec id="s4" sec-type="methods"><title>Methods</title><sec id="s4-1"><title>Food choice task</title><p>A total of 30 participants completed the snack task, which consisted of a rating and a choice phase. The experimental procedures were approved by the Institutional Review Board (IRB) at Columbia University, and participants provided signed informed consent before participating in the study. The data were previously published in <xref ref-type="bibr" rid="bib5">Bakkour et al., 2019</xref>.</p><sec id="s4-1-1"><title>Rating phase</title><p>Participants were shown a series of snack items in a randomized order on a computer screen. They indicated their willingness to pay (WTP) by using the computer mouse to move a cursor along an analog scale ranging from $0 to $3 at the bottom of the screen. The process was self-paced, and each snack item was presented one at a time. After completing the ratings for all 60 items, participants were given the opportunity to revise their ratings. The 60 items were re-displayed in random order, with the original bids displayed below each item. Participants either chose to keep their original bid by clicking ‘NO’ or to revise the bid by clicking ‘YES’, which re-displayed the analog scale for bid adjustment. We take the final WTP that is reported for each item as the corresponding <italic>static</italic> value (<italic>s-value</italic>).</p></sec><sec id="s4-1-2"><title>Choice phase</title><p>From the 60 rated items, 150 unique pairs were formed, ensuring variation in <inline-formula><mml:math id="inf83"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>s</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula>. Each of the 60 items was included in five different pairs. Sixty item pairs were presented twice, resulting in a total of 210 trials per participant. Item pairs were presented in random order, with one item on each side of a central fixation cross. Participants were instructed to select their preferred food item and were informed that they would receive their chosen food from a randomly selected trial to consume at the end of the experiment. The task took place in an MRI scanner. Participants indicated their choice on each trial by pressing one of two buttons on an MRI-compatible button box. They had up to 3 s to make their choice. Once a choice was made, the chosen item was highlighted for 500ms. Trials were separated by an inter-trial interval (ITI) drawn from a truncated exponential distribution with a minimum ITI of 1 and a maximum ITI of 12 s. The resulting distribution of ITIs across trials had a true mean of 3.05 s and a standard deviation of 2.0 s.</p></sec></sec><sec id="s4-2"><title>Data analysis</title><p>Association between the <italic>s-values</italic>, choice and RT. We used the following logistic regression model to evaluate the association between the <italic>s-values</italic> and the probability of choosing the item on the right:<disp-formula id="equ2"><label>(2)</label><mml:math id="m2"><mml:mrow><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mrow><mml:mi mathvariant="normal">l</mml:mi><mml:mi mathvariant="normal">o</mml:mi><mml:mi mathvariant="normal">g</mml:mi><mml:mi mathvariant="normal">i</mml:mi><mml:mi mathvariant="normal">t</mml:mi></mml:mrow><mml:mo stretchy="false">[</mml:mo><mml:msub><mml:mi>p</mml:mi><mml:mrow><mml:mrow><mml:mi mathvariant="normal">r</mml:mi><mml:mi mathvariant="normal">i</mml:mi><mml:mi mathvariant="normal">g</mml:mi><mml:mi mathvariant="normal">h</mml:mi><mml:mi mathvariant="normal">t</mml:mi></mml:mrow></mml:mrow></mml:msub><mml:mo stretchy="false">]</mml:mo><mml:mo>=</mml:mo><mml:munderover><mml:mo>∑</mml:mo><mml:mrow><mml:mi>i</mml:mi><mml:mo>=</mml:mo><mml:mn>1</mml:mn></mml:mrow><mml:mrow><mml:msub><mml:mi>N</mml:mi><mml:mrow><mml:mrow><mml:mi mathvariant="normal">s</mml:mi><mml:mi mathvariant="normal">u</mml:mi><mml:mi mathvariant="normal">b</mml:mi><mml:mi mathvariant="normal">j</mml:mi></mml:mrow></mml:mrow></mml:msub></mml:mrow></mml:munderover><mml:msub><mml:mi>β</mml:mi><mml:mrow><mml:mn>0</mml:mn><mml:mo>,</mml:mo><mml:mi>i</mml:mi></mml:mrow></mml:msub><mml:msub><mml:mi>I</mml:mi><mml:mrow><mml:mrow><mml:mi mathvariant="normal">i</mml:mi></mml:mrow></mml:mrow></mml:msub><mml:mo>+</mml:mo><mml:msub><mml:mi>β</mml:mi><mml:mrow><mml:mn>1</mml:mn></mml:mrow></mml:msub><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow><mml:mi>s</mml:mi></mml:mrow></mml:msub><mml:mo>,</mml:mo></mml:mstyle></mml:mrow></mml:math></disp-formula></p><p>where <inline-formula><mml:math id="inf84"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msub><mml:mi>I</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi mathvariant="normal">i</mml:mi></mml:mrow></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula> is an indicator variable that takes the value 1 if the trial was completed by subject <inline-formula><mml:math id="inf85"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>i</mml:mi></mml:mstyle></mml:math></inline-formula> and 0 otherwise. We used a t-test to evaluate the hypothesis that the corresponding regression coefficient is zero, using the standard error of the estimated regression coefficient.</p><p>Similarly, we used a linear regression model to test the influence of <inline-formula><mml:math id="inf86"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>s</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula> on response times:<disp-formula id="equ3"><label>(3)</label><mml:math id="m3"><mml:mrow><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mrow><mml:mi mathvariant="normal">R</mml:mi><mml:mi mathvariant="normal">T</mml:mi></mml:mrow><mml:mo>=</mml:mo><mml:munderover><mml:mo>∑</mml:mo><mml:mrow><mml:mi>i</mml:mi><mml:mo>=</mml:mo><mml:mn>1</mml:mn></mml:mrow><mml:mrow><mml:msub><mml:mi>N</mml:mi><mml:mrow><mml:mrow><mml:mi mathvariant="normal">s</mml:mi><mml:mi mathvariant="normal">u</mml:mi><mml:mi mathvariant="normal">b</mml:mi><mml:mi mathvariant="normal">j</mml:mi></mml:mrow></mml:mrow></mml:msub></mml:mrow></mml:munderover><mml:msub><mml:mi>β</mml:mi><mml:mrow><mml:mn>0</mml:mn><mml:mo>,</mml:mo><mml:mi>i</mml:mi></mml:mrow></mml:msub><mml:msub><mml:mi>I</mml:mi><mml:mrow><mml:mrow><mml:mi mathvariant="normal">i</mml:mi></mml:mrow></mml:mrow></mml:msub><mml:mo>+</mml:mo><mml:msub><mml:mi>β</mml:mi><mml:mrow><mml:mn>1</mml:mn></mml:mrow></mml:msub><mml:mrow><mml:mo>|</mml:mo><mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow><mml:mi>s</mml:mi></mml:mrow></mml:msub></mml:mrow><mml:mo>|</mml:mo></mml:mrow><mml:mo>+</mml:mo><mml:msub><mml:mi>β</mml:mi><mml:mrow><mml:mn>2</mml:mn></mml:mrow></mml:msub><mml:mi mathvariant="normal">Σ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow><mml:mi>s</mml:mi></mml:mrow></mml:msub><mml:mo>,</mml:mo></mml:mstyle></mml:mrow></mml:math></disp-formula></p><p>where <inline-formula><mml:math id="inf87"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mrow class="MJX-TeXAtom-ORD"><mml:mo stretchy="false">|</mml:mo></mml:mrow><mml:mo>⋅</mml:mo><mml:mrow class="MJX-TeXAtom-ORD"><mml:mo stretchy="false">|</mml:mo></mml:mrow></mml:mstyle></mml:math></inline-formula> denotes absolute value and <inline-formula><mml:math id="inf88"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Σ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>s</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula> is the sum of the value of the two items presented on each trial. The last term was included to account for the potential influence of value sum on response time (<xref ref-type="bibr" rid="bib66">Smith and Krajbich, 2019</xref>).</p><sec id="s4-2-1"><title>Predicting choices in <italic>cynosure</italic> trials</title><p>We used two logistic regression models to predict the choice in each trial using observations from the other trials. We refer to the trial under consideration as the <italic>cynosure</italic> trial (<xref ref-type="fig" rid="fig2">Figure 2</xref>). One model uses the explicitly reported values:<disp-formula id="equ4"><label>(4)</label><mml:math id="m4"><mml:mrow><mml:mrow><mml:mi mathvariant="normal">l</mml:mi><mml:mi mathvariant="normal">o</mml:mi><mml:mi mathvariant="normal">g</mml:mi><mml:mi mathvariant="normal">i</mml:mi><mml:mi mathvariant="normal">t</mml:mi></mml:mrow><mml:mo stretchy="false">[</mml:mo><mml:msub><mml:mi>p</mml:mi><mml:mrow><mml:mrow><mml:mi mathvariant="normal">r</mml:mi><mml:mi mathvariant="normal">i</mml:mi><mml:mi mathvariant="normal">g</mml:mi><mml:mi mathvariant="normal">h</mml:mi><mml:mi mathvariant="normal">t</mml:mi></mml:mrow></mml:mrow></mml:msub><mml:mo stretchy="false">]</mml:mo><mml:mo>=</mml:mo><mml:msub><mml:mi>β</mml:mi><mml:mrow><mml:mn>0</mml:mn></mml:mrow></mml:msub><mml:mo>+</mml:mo><mml:msub><mml:mi>β</mml:mi><mml:mrow><mml:mn>1</mml:mn></mml:mrow></mml:msub><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow><mml:mi>s</mml:mi></mml:mrow></mml:msub><mml:mo>,</mml:mo></mml:mrow></mml:math></disp-formula></p><p>while the other model uses the choices made on other trials:<disp-formula id="equ5"><label>(5)</label><mml:math id="m5"><mml:mrow><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mrow><mml:mi mathvariant="normal">l</mml:mi><mml:mi mathvariant="normal">o</mml:mi><mml:mi mathvariant="normal">g</mml:mi><mml:mi mathvariant="normal">i</mml:mi><mml:mi mathvariant="normal">t</mml:mi></mml:mrow><mml:mo stretchy="false">[</mml:mo><mml:msub><mml:mi>p</mml:mi><mml:mrow><mml:mrow><mml:mi mathvariant="normal">r</mml:mi><mml:mi mathvariant="normal">i</mml:mi><mml:mi mathvariant="normal">g</mml:mi><mml:mi mathvariant="normal">h</mml:mi><mml:mi mathvariant="normal">t</mml:mi></mml:mrow></mml:mrow></mml:msub><mml:mo stretchy="false">]</mml:mo><mml:mo>=</mml:mo><mml:msub><mml:mi>β</mml:mi><mml:mn>0</mml:mn></mml:msub><mml:mo>+</mml:mo><mml:munderover><mml:mo>∑</mml:mo><mml:mrow><mml:mi>i</mml:mi><mml:mo>=</mml:mo><mml:mn>1</mml:mn></mml:mrow><mml:mrow><mml:msub><mml:mi>N</mml:mi><mml:mrow><mml:mrow><mml:mi mathvariant="normal">i</mml:mi><mml:mi mathvariant="normal">t</mml:mi><mml:mi mathvariant="normal">e</mml:mi><mml:mi mathvariant="normal">m</mml:mi><mml:mi mathvariant="normal">s</mml:mi></mml:mrow></mml:mrow></mml:msub></mml:mrow></mml:munderover><mml:msub><mml:mi>β</mml:mi><mml:mrow><mml:mi>i</mml:mi></mml:mrow></mml:msub><mml:mi>f</mml:mi><mml:mo stretchy="false">(</mml:mo><mml:mi>i</mml:mi><mml:mo stretchy="false">)</mml:mo><mml:mo>,</mml:mo></mml:mstyle></mml:mrow></mml:math></disp-formula></p><p>where<disp-formula id="equ6"><label>(6)</label><mml:math id="m6"><mml:mrow><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>f</mml:mi><mml:mo stretchy="false">(</mml:mo><mml:mi>i</mml:mi><mml:mo stretchy="false">)</mml:mo><mml:mo>=</mml:mo><mml:mrow><mml:mo>{</mml:mo><mml:mtable columnalign="left left" rowspacing=".2em" columnspacing="1em" displaystyle="false"><mml:mtr><mml:mtd><mml:mn>1</mml:mn></mml:mtd><mml:mtd><mml:mstyle displaystyle="false" scriptlevel="0"><mml:mtext>if item </mml:mtext><mml:mrow><mml:mi>i</mml:mi></mml:mrow><mml:mtext> is on the right</mml:mtext></mml:mstyle></mml:mtd></mml:mtr><mml:mtr><mml:mtd><mml:mo>−</mml:mo><mml:mn>1</mml:mn></mml:mtd><mml:mtd><mml:mstyle displaystyle="false" scriptlevel="0"><mml:mtext>if item </mml:mtext><mml:mrow><mml:mi>i</mml:mi></mml:mrow><mml:mtext> is on the left</mml:mtext></mml:mstyle></mml:mtd></mml:mtr><mml:mtr><mml:mtd><mml:mn>0</mml:mn></mml:mtd><mml:mtd><mml:mstyle displaystyle="false" scriptlevel="0"><mml:mtext>otherwise</mml:mtext></mml:mstyle></mml:mtd></mml:mtr></mml:mtable><mml:mo fence="true" stretchy="true" symmetric="true"/></mml:mrow></mml:mstyle></mml:mrow></mml:math></disp-formula></p><p>For this model, we included an L2 regularization with <inline-formula><mml:math id="inf89"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>λ</mml:mi><mml:mo>=</mml:mo><mml:mn>0.5</mml:mn></mml:mstyle></mml:math></inline-formula>. Both models were fit independently for each participant. We only included trials with the first appearance of each item pair (i.e. we did not include the repeated trials) so that the choice prediction for the <italic>cynosure</italic> trial is not influenced by the choice made in the paired trial containing the same items as in the <italic>cynosure</italic> trial.</p><p>Association between <italic>d-values</italic> and choice. We tested the association between <italic>d-values</italic> and choice with a logistic regression model fit to the choices. We included separate regressors for <inline-formula><mml:math id="inf90"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>d</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula> and <inline-formula><mml:math id="inf91"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>s</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula>:<disp-formula id="equ7"><label>(7)</label><mml:math id="m7"><mml:mrow><mml:mrow><mml:mi mathvariant="normal">l</mml:mi><mml:mi mathvariant="normal">o</mml:mi><mml:mi mathvariant="normal">g</mml:mi><mml:mi mathvariant="normal">i</mml:mi><mml:mi mathvariant="normal">t</mml:mi></mml:mrow><mml:mo stretchy="false">[</mml:mo><mml:msub><mml:mi>p</mml:mi><mml:mrow><mml:mrow><mml:mi mathvariant="normal">r</mml:mi><mml:mi mathvariant="normal">i</mml:mi><mml:mi mathvariant="normal">g</mml:mi><mml:mi mathvariant="normal">h</mml:mi><mml:mi mathvariant="normal">t</mml:mi></mml:mrow></mml:mrow></mml:msub><mml:mo stretchy="false">]</mml:mo><mml:mo>=</mml:mo><mml:msub><mml:mi>β</mml:mi><mml:mrow><mml:mn>0</mml:mn></mml:mrow></mml:msub><mml:mo>+</mml:mo><mml:msub><mml:mi>β</mml:mi><mml:mrow><mml:mi>s</mml:mi></mml:mrow></mml:msub><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow><mml:mi>s</mml:mi></mml:mrow></mml:msub><mml:mo>+</mml:mo><mml:msub><mml:mi>β</mml:mi><mml:mrow><mml:mi>d</mml:mi></mml:mrow></mml:msub><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow><mml:mi>d</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:math></disp-formula></p><p>The model was fit separately for each participant. <xref ref-type="fig" rid="fig5s1">Figure 5—figure supplement 1</xref> shows the regression coefficients associated with <inline-formula><mml:math id="inf92"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>s</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula> and <inline-formula><mml:math id="inf93"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>d</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula>.</p></sec><sec id="s4-2-2"><title>Choice and response time functions</title><p>When plotting the psychometric and chronometric functions (e.g., <xref ref-type="fig" rid="fig1">Figure 1C–D</xref>), we binned trials depending on the value of <inline-formula><mml:math id="inf94"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>s</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula> (or <inline-formula><mml:math id="inf95"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>d</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula>). The bins are defined by the following edges: { <inline-formula><mml:math id="inf96"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mo>−</mml:mo><mml:mi mathvariant="normal">∞</mml:mi></mml:mstyle></mml:math></inline-formula>,−1.5,–0.75,−0.375,–0.1875,–0.0625, 0.0625,0.1875,0.375,0.75,1.5,<inline-formula><mml:math id="inf97"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">∞</mml:mi></mml:mstyle></mml:math></inline-formula> }. We averaged the choice or RT for the trials (grouped across participants) within each bin and plotted them aligned to the mean <inline-formula><mml:math id="inf98"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>x</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula> of each bin.</p></sec><sec id="s4-2-3"><title>Match probability</title><p>We used logistic regression to determine if the probability of giving the same response to the pair of trials with identical stimuli depended on the number of trials in between (<xref ref-type="fig" rid="fig3">Figure 3</xref>). The model is:<disp-formula id="equ8"><label>(8)</label><mml:math id="m8"><mml:mrow><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mrow><mml:mi mathvariant="normal">l</mml:mi><mml:mi mathvariant="normal">o</mml:mi><mml:mi mathvariant="normal">g</mml:mi><mml:mi mathvariant="normal">i</mml:mi><mml:mi mathvariant="normal">t</mml:mi></mml:mrow><mml:mo stretchy="false">[</mml:mo><mml:msub><mml:mi>p</mml:mi><mml:mrow><mml:mi>m</mml:mi><mml:mi>a</mml:mi><mml:mi>t</mml:mi><mml:mi>c</mml:mi><mml:mi>h</mml:mi></mml:mrow></mml:msub><mml:mo stretchy="false">]</mml:mo><mml:mo>=</mml:mo><mml:munderover><mml:mo>∑</mml:mo><mml:mrow><mml:mi>i</mml:mi><mml:mo>=</mml:mo><mml:mn>1</mml:mn></mml:mrow><mml:mrow><mml:msub><mml:mi>N</mml:mi><mml:mrow><mml:mrow><mml:mi mathvariant="normal">s</mml:mi><mml:mi mathvariant="normal">u</mml:mi><mml:mi mathvariant="normal">b</mml:mi><mml:mi mathvariant="normal">j</mml:mi></mml:mrow></mml:mrow></mml:msub></mml:mrow></mml:munderover><mml:msub><mml:mi>β</mml:mi><mml:mrow><mml:mn>0</mml:mn><mml:mo>,</mml:mo><mml:mi>i</mml:mi></mml:mrow></mml:msub><mml:msub><mml:mi>I</mml:mi><mml:mrow><mml:mrow><mml:mi mathvariant="normal">i</mml:mi></mml:mrow></mml:mrow></mml:msub><mml:mo>+</mml:mo><mml:munderover><mml:mo>∑</mml:mo><mml:mrow><mml:mi>i</mml:mi><mml:mo>=</mml:mo><mml:mn>1</mml:mn></mml:mrow><mml:mrow><mml:msub><mml:mi>N</mml:mi><mml:mrow><mml:mrow><mml:mi mathvariant="normal">s</mml:mi><mml:mi mathvariant="normal">u</mml:mi><mml:mi mathvariant="normal">b</mml:mi><mml:mi mathvariant="normal">j</mml:mi></mml:mrow></mml:mrow></mml:msub></mml:mrow></mml:munderover><mml:msub><mml:mi>β</mml:mi><mml:mrow><mml:mn>1</mml:mn><mml:mo>,</mml:mo><mml:mi>i</mml:mi></mml:mrow></mml:msub><mml:msub><mml:mi>I</mml:mi><mml:mrow><mml:mrow><mml:mi mathvariant="normal">i</mml:mi></mml:mrow></mml:mrow></mml:msub><mml:mrow><mml:mo stretchy="false">|</mml:mo></mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mi>s</mml:mi></mml:msub><mml:mrow><mml:mo stretchy="false">|</mml:mo></mml:mrow><mml:mo>+</mml:mo><mml:msub><mml:mi>β</mml:mi><mml:mn>2</mml:mn></mml:msub><mml:mrow><mml:mo>(</mml:mo><mml:mrow><mml:msub><mml:mrow><mml:mi mathvariant="normal">T</mml:mi></mml:mrow><mml:mrow><mml:mn>2</mml:mn><mml:mi>n</mml:mi><mml:mi>d</mml:mi></mml:mrow></mml:msub><mml:mo>−</mml:mo><mml:msub><mml:mrow><mml:mi mathvariant="normal">T</mml:mi></mml:mrow><mml:mrow><mml:mn>1</mml:mn><mml:mi>s</mml:mi><mml:mi>t</mml:mi></mml:mrow></mml:msub></mml:mrow><mml:mo>)</mml:mo></mml:mrow></mml:mstyle></mml:mrow></mml:math></disp-formula></p><p>where <inline-formula><mml:math id="inf99"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msub><mml:mi>p</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>m</mml:mi><mml:mi>a</mml:mi><mml:mi>t</mml:mi><mml:mi>c</mml:mi><mml:mi>h</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula> is the probability of choosing the same item on both occasions, <inline-formula><mml:math id="inf100"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msub><mml:mi>I</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi mathvariant="normal">i</mml:mi></mml:mrow></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula> is an indicator variable that takes a value of 1 if the pair of trials correspond to subject <inline-formula><mml:math id="inf101"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>i</mml:mi></mml:mstyle></mml:math></inline-formula>, and zero otherwise, and <inline-formula><mml:math id="inf102"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msub><mml:mi>T</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mn>1</mml:mn><mml:mi>s</mml:mi><mml:mi>t</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula> and <inline-formula><mml:math id="inf103"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msub><mml:mi>T</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mn>2</mml:mn><mml:mi>n</mml:mi><mml:mi>d</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula> are the trial number of the first and second occurrences of the same pair, respectively. We used a t-test to evaluate the hypothesis that <inline-formula><mml:math id="inf104"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msub><mml:mi>β</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mn>2</mml:mn></mml:mrow></mml:msub><mml:mo>=</mml:mo><mml:mn>0</mml:mn></mml:mstyle></mml:math></inline-formula> (i.e., that the separation between trials with identical stimuli had no effect on <inline-formula><mml:math id="inf105"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msub><mml:mi>p</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi mathvariant="normal">m</mml:mi><mml:mi mathvariant="normal">a</mml:mi><mml:mi mathvariant="normal">t</mml:mi><mml:mi mathvariant="normal">c</mml:mi><mml:mi mathvariant="normal">h</mml:mi></mml:mrow></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula>).</p></sec></sec><sec id="s4-3"><title>Drift-diffusion model</title><p>We fit the choice and RT data with a drift-diffusion model. It assumes that the decision variable, <inline-formula><mml:math id="inf106"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>x</mml:mi></mml:mstyle></mml:math></inline-formula>, is given by the accumulation of signal and noise, where the signal is a function of the difference in value between the items, <inline-formula><mml:math id="inf107"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:mi>v</mml:mi></mml:mstyle></mml:math></inline-formula>, and the noise is equal to <inline-formula><mml:math id="inf108"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msqrt><mml:mi>d</mml:mi><mml:mi>t</mml:mi></mml:msqrt></mml:mstyle></mml:math></inline-formula>, where <inline-formula><mml:math id="inf109"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>d</mml:mi><mml:mi>t</mml:mi></mml:mstyle></mml:math></inline-formula> is the time step, such that the accumulated noise after 1 s of unbounded accumulation, the variance of the accumulated noise is equal to 1. The decision variable follows the difference equation,<disp-formula id="equ9"><label>(9)</label><mml:math id="m9"><mml:mrow><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msub><mml:mi>x</mml:mi><mml:mrow><mml:mi>t</mml:mi><mml:mo>+</mml:mo><mml:mn>1</mml:mn></mml:mrow></mml:msub><mml:mo>=</mml:mo><mml:msub><mml:mi>x</mml:mi><mml:mi>t</mml:mi></mml:msub><mml:mo>+</mml:mo><mml:mi>κ</mml:mi><mml:mtext> </mml:mtext><mml:mi>d</mml:mi><mml:mi>t</mml:mi><mml:mtext> </mml:mtext><mml:mo stretchy="false">(</mml:mo><mml:mi>μ</mml:mi><mml:mrow><mml:mo>+</mml:mo></mml:mrow><mml:msub><mml:mi>μ</mml:mi><mml:mn>0</mml:mn></mml:msub><mml:mo stretchy="false">)</mml:mo><mml:mo>+</mml:mo><mml:msqrt><mml:mi>d</mml:mi><mml:mi>t</mml:mi></mml:msqrt><mml:mspace width="thinmathspace"/><mml:msub><mml:mi>η</mml:mi><mml:mi>t</mml:mi></mml:msub><mml:mo>,</mml:mo></mml:mstyle></mml:mrow></mml:math></disp-formula></p><p>where <inline-formula><mml:math id="inf110"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msub><mml:mi>η</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>t</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula> is sampled from a normal distribution with a mean 0 and variance 1, <inline-formula><mml:math id="inf111"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>κ</mml:mi></mml:mstyle></mml:math></inline-formula> is a signal-noise parameter, μ is the drift rate and <inline-formula><mml:math id="inf112"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msub><mml:mi>μ</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mn>0</mml:mn></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula> is a bias coefficient that is included to account for potential asymmetries between right and left choices.</p><p>We assume that the drift rate is a (potentially nonlinear) function of <inline-formula><mml:math id="inf113"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mrow><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:mi>v</mml:mi></mml:mstyle></mml:mrow></mml:mstyle></mml:math></inline-formula>. We parameterize this relationship as a power law, so that<disp-formula id="equ10"><label>(10)</label><mml:math id="m10"><mml:mrow><mml:mi>μ</mml:mi><mml:mo>=</mml:mo><mml:mrow><mml:mi mathvariant="normal">s</mml:mi><mml:mi mathvariant="normal">i</mml:mi><mml:mi mathvariant="normal">g</mml:mi><mml:mi mathvariant="normal">n</mml:mi></mml:mrow><mml:mo stretchy="false">(</mml:mo><mml:mi mathvariant="normal">Δ</mml:mi><mml:mi>v</mml:mi><mml:mo stretchy="false">)</mml:mo><mml:mrow><mml:mo stretchy="false">|</mml:mo></mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:mi>v</mml:mi><mml:msup><mml:mrow><mml:mo stretchy="false">|</mml:mo></mml:mrow><mml:mrow><mml:mi>γ</mml:mi></mml:mrow></mml:msup><mml:mo>,</mml:mo></mml:mrow></mml:math></disp-formula></p><p>where <inline-formula><mml:math id="inf114"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi mathvariant="normal">s</mml:mi><mml:mi mathvariant="normal">i</mml:mi><mml:mi mathvariant="normal">g</mml:mi><mml:mi mathvariant="normal">n</mml:mi></mml:mrow></mml:mstyle></mml:math></inline-formula> is the sign operation, <inline-formula><mml:math id="inf115"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mrow class="MJX-TeXAtom-ORD"><mml:mo stretchy="false">|</mml:mo></mml:mrow><mml:mrow class="MJX-TeXAtom-ORD"><mml:mo stretchy="false">|</mml:mo></mml:mrow></mml:mstyle></mml:math></inline-formula> indicates absolute value, and <inline-formula><mml:math id="inf116"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>γ</mml:mi></mml:mstyle></mml:math></inline-formula> is a fit parameter.</p><p>The decision terminates when the accumulated evidence reaches an upper bound, signaling a rightward choice, or a lower bound, signaling a leftward choice. The bound is assumed to collapse over time. It is constant until time <inline-formula><mml:math id="inf117"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>d</mml:mi></mml:mstyle></mml:math></inline-formula>, and then it collapses at rate <inline-formula><mml:math id="inf118"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>a</mml:mi></mml:mstyle></mml:math></inline-formula>:<disp-formula id="equ11"><label>(11)</label><mml:math id="m11"><mml:mrow><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>B</mml:mi><mml:mo stretchy="false">(</mml:mo><mml:mi>t</mml:mi><mml:mo stretchy="false">)</mml:mo><mml:mo>=</mml:mo><mml:mo>±</mml:mo><mml:mrow><mml:mo>{</mml:mo><mml:mtable columnalign="left left" rowspacing=".2em" columnspacing="1em" displaystyle="false"><mml:mtr><mml:mtd><mml:msub><mml:mi>B</mml:mi><mml:mn>0</mml:mn></mml:msub></mml:mtd><mml:mtd><mml:mrow><mml:mtext>if </mml:mtext><mml:mrow><mml:mi>t</mml:mi><mml:mo>&lt;</mml:mo><mml:mi>d</mml:mi></mml:mrow></mml:mrow></mml:mtd></mml:mtr><mml:mtr><mml:mtd><mml:msub><mml:mi>B</mml:mi><mml:mn>0</mml:mn></mml:msub><mml:msup><mml:mtext>exp</mml:mtext><mml:mrow><mml:mo>−</mml:mo><mml:mi>a</mml:mi><mml:mo stretchy="false">(</mml:mo><mml:mi>t</mml:mi><mml:mo>−</mml:mo><mml:mi>d</mml:mi><mml:mo stretchy="false">)</mml:mo></mml:mrow></mml:msup></mml:mtd><mml:mtd><mml:mtext>otherwise</mml:mtext><mml:mo>.</mml:mo></mml:mtd></mml:mtr></mml:mtable><mml:mo fence="true" stretchy="true" symmetric="true"/></mml:mrow></mml:mstyle></mml:mrow></mml:math></disp-formula></p><p>Collapsing bounds are needed to explain why choices that are consistent with the value ratings are usually faster than inconsistent choices for the same <inline-formula><mml:math id="inf119"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mrow><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:mi>v</mml:mi></mml:mstyle></mml:mrow></mml:mstyle></mml:math></inline-formula>.</p><p>The response time is the sum of the the decision time, given by the time taken by the diffusing particle to reach of the bounds, and a non-decision time which is assumed to be normally distributed with mean <inline-formula><mml:math id="inf120"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msub><mml:mi>μ</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>n</mml:mi><mml:mi>d</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula> and standard deviation <inline-formula><mml:math id="inf121"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msub><mml:mi>σ</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>n</mml:mi><mml:mi>d</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula>.</p><p>The model has 8 parameters: <inline-formula><mml:math id="inf122"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mo fence="false" stretchy="false">{</mml:mo><mml:mi>κ</mml:mi><mml:mo>,</mml:mo><mml:msub><mml:mi>B</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mn>0</mml:mn></mml:mrow></mml:msub><mml:mo>,</mml:mo><mml:mi>a</mml:mi><mml:mo>,</mml:mo><mml:mi>d</mml:mi><mml:mo>,</mml:mo><mml:mi>γ</mml:mi><mml:mo>,</mml:mo><mml:msub><mml:mi>μ</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mn>0</mml:mn></mml:mrow></mml:msub><mml:mo>,</mml:mo><mml:msub><mml:mi>μ</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>n</mml:mi><mml:mi>d</mml:mi></mml:mrow></mml:msub><mml:mo>,</mml:mo><mml:msub><mml:mi>σ</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>n</mml:mi><mml:mi>d</mml:mi></mml:mrow></mml:msub><mml:mo fence="false" stretchy="false">}</mml:mo></mml:mstyle></mml:math></inline-formula>. The standard deviation of the non-decision times (<inline-formula><mml:math id="inf123"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msub><mml:mi>σ</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>n</mml:mi><mml:mi>d</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula>) was fixed to <inline-formula><mml:math id="inf124"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mn>0.05</mml:mn></mml:mstyle></mml:math></inline-formula> s. For the fits shown in <xref ref-type="fig" rid="fig1">Figures 1C–D </xref>–<xref ref-type="fig" rid="fig5">5A</xref>, we fit the model to grouped data from all participants. For the analysis of variance explained (<xref ref-type="fig" rid="fig5">Figure 5</xref>) and model comparison (<xref ref-type="fig" rid="fig5s2">Figure 5—figure supplement 2</xref>), we fit the model separately for each participant. The model was fit to maximize the log of the likelihood of the parameters given the single-trial choice and RT:<disp-formula id="equ12"><label>(12)</label><mml:math id="m12"><mml:mrow><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mrow><mml:mtext>log L</mml:mtext></mml:mrow><mml:mo stretchy="false">(</mml:mo><mml:mrow><mml:mi mathvariant="normal">p</mml:mi><mml:mi mathvariant="normal">a</mml:mi><mml:mi mathvariant="normal">r</mml:mi><mml:mi mathvariant="normal">a</mml:mi><mml:mi mathvariant="normal">m</mml:mi><mml:mi mathvariant="normal">e</mml:mi><mml:mi mathvariant="normal">t</mml:mi><mml:mi mathvariant="normal">e</mml:mi><mml:mi mathvariant="normal">r</mml:mi><mml:mi mathvariant="normal">s</mml:mi></mml:mrow><mml:mo stretchy="false">)</mml:mo><mml:mo>=</mml:mo><mml:munderover><mml:mo>∑</mml:mo><mml:mrow><mml:mi>i</mml:mi><mml:mo>=</mml:mo><mml:mn>1</mml:mn></mml:mrow><mml:mrow><mml:msub><mml:mi>n</mml:mi><mml:mrow><mml:mrow><mml:mi mathvariant="normal">t</mml:mi><mml:mi mathvariant="normal">r</mml:mi><mml:mi mathvariant="normal">i</mml:mi><mml:mi mathvariant="normal">a</mml:mi><mml:mi mathvariant="normal">l</mml:mi><mml:mi mathvariant="normal">s</mml:mi></mml:mrow></mml:mrow></mml:msub></mml:mrow></mml:munderover><mml:mrow><mml:mi mathvariant="normal">l</mml:mi><mml:mi mathvariant="normal">o</mml:mi><mml:mi mathvariant="normal">g</mml:mi></mml:mrow><mml:mrow><mml:mo>(</mml:mo><mml:mrow><mml:mi>p</mml:mi><mml:mrow><mml:mo>(</mml:mo><mml:mrow><mml:msup><mml:mrow><mml:mi mathvariant="normal">c</mml:mi><mml:mi mathvariant="normal">h</mml:mi><mml:mi mathvariant="normal">o</mml:mi><mml:mi mathvariant="normal">i</mml:mi><mml:mi mathvariant="normal">c</mml:mi><mml:mi mathvariant="normal">e</mml:mi></mml:mrow><mml:mrow><mml:mo stretchy="false">(</mml:mo><mml:mi>i</mml:mi><mml:mo stretchy="false">)</mml:mo></mml:mrow></mml:msup><mml:mo>,</mml:mo><mml:msup><mml:mrow><mml:mi mathvariant="normal">R</mml:mi><mml:mi mathvariant="normal">T</mml:mi></mml:mrow><mml:mrow><mml:mo stretchy="false">(</mml:mo><mml:mi>i</mml:mi><mml:mo stretchy="false">)</mml:mo></mml:mrow></mml:msup><mml:mrow><mml:mo stretchy="false">|</mml:mo></mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:msup><mml:mi>v</mml:mi><mml:mrow><mml:mo stretchy="false">(</mml:mo><mml:mi>i</mml:mi><mml:mo stretchy="false">)</mml:mo></mml:mrow></mml:msup><mml:mo>,</mml:mo><mml:mrow><mml:mi mathvariant="normal">p</mml:mi><mml:mi mathvariant="normal">a</mml:mi><mml:mi mathvariant="normal">r</mml:mi><mml:mi mathvariant="normal">a</mml:mi><mml:mi mathvariant="normal">m</mml:mi><mml:mi mathvariant="normal">e</mml:mi><mml:mi mathvariant="normal">t</mml:mi><mml:mi mathvariant="normal">e</mml:mi><mml:mi mathvariant="normal">r</mml:mi><mml:mi mathvariant="normal">s</mml:mi></mml:mrow></mml:mrow><mml:mo>)</mml:mo></mml:mrow></mml:mrow><mml:mo>)</mml:mo></mml:mrow><mml:mo>.</mml:mo></mml:mstyle></mml:mrow></mml:math></disp-formula></p><p>We evaluate the likelihood by numerically solving the Fokker-Planck (FP) equation that described the dynamics of the drift-diffusion process, using the Chang-Cooper fully-implicit method (<xref ref-type="bibr" rid="bib15">Chang and Cooper, 1970</xref>; <xref ref-type="bibr" rid="bib41">Kiani and Shadlen, 2009</xref>; <xref ref-type="bibr" rid="bib78">Zylberberg et al., 2016</xref>). For computational considerations, we bin the values of <inline-formula><mml:math id="inf125"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mrow><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi mathvariant="normal">Δ</mml:mi><mml:mi>v</mml:mi></mml:mstyle></mml:mrow></mml:mstyle></mml:math></inline-formula> to multiples of $0.1. From the numerical solution of the FP equation, we obtain the distribution of decision times, which is convolved with the truncated Gaussian distribution of non-decision latencies. The truncation ensures that the non-decision times are non-negative, which could otherwise occur during the optimization process for large values of <inline-formula><mml:math id="inf126"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msub><mml:mi>σ</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>n</mml:mi><mml:mi>d</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula>. The parameter search was performed using the Bayesian Adaptive Direct Search (BADS) algorithm (<xref ref-type="bibr" rid="bib3">Acerbi and Ma, 2017</xref>).</p></sec><sec id="s4-4"><title>Revaluation algorithm</title><p>The <italic>Reval</italic> algorithm was applied to each participant independently. The values are initialized to those reported during the ratings phase. They are then revised, based on the outcome of each trial, in the order of the experiment.</p><p>The value of the chosen item is increased by <inline-formula><mml:math id="inf127"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>δ</mml:mi></mml:mstyle></mml:math></inline-formula> and the value of the unchosen item is decreased by the same amount. The revaluation affects future decisions in which the same item is presented.</p><p>We searched for the value of <inline-formula><mml:math id="inf128"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msup><mml:mi>δ</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mo>∗</mml:mo></mml:mrow></mml:msup></mml:mstyle></mml:math></inline-formula> that minimizes the deviance of the logistic regression model specified by <xref ref-type="disp-formula" rid="equ1">Equation 1</xref>. The model’s deviance is given by:<disp-formula id="equ13"><label>(13)</label><mml:math id="m13"><mml:mrow><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mrow><mml:mi mathvariant="normal">D</mml:mi><mml:mi mathvariant="normal">E</mml:mi><mml:mi mathvariant="normal">V</mml:mi></mml:mrow><mml:mo>=</mml:mo><mml:munderover><mml:mo>∑</mml:mo><mml:mrow><mml:mi>i</mml:mi><mml:mo>=</mml:mo><mml:mn>1</mml:mn></mml:mrow><mml:mrow><mml:msub><mml:mi>N</mml:mi><mml:mrow><mml:mrow><mml:mi mathvariant="normal">t</mml:mi><mml:mi mathvariant="normal">r</mml:mi></mml:mrow></mml:mrow></mml:msub></mml:mrow></mml:munderover><mml:mn>2</mml:mn><mml:mtext> </mml:mtext><mml:mrow><mml:mi mathvariant="normal">l</mml:mi><mml:mi mathvariant="normal">o</mml:mi><mml:msub><mml:mi mathvariant="normal">g</mml:mi><mml:mi mathvariant="normal">e</mml:mi></mml:msub></mml:mrow><mml:mrow><mml:mrow><mml:mo>(</mml:mo><mml:mfrac><mml:mn>1</mml:mn><mml:msub><mml:mrow><mml:mover><mml:mi>c</mml:mi><mml:mo stretchy="false">^</mml:mo></mml:mover></mml:mrow><mml:mi>i</mml:mi></mml:msub></mml:mfrac><mml:mo>)</mml:mo></mml:mrow></mml:mrow></mml:mstyle></mml:mrow></mml:math></disp-formula></p><p>where the sum is over trials and <inline-formula><mml:math id="inf129"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mrow class="MJX-TeXAtom-ORD"><mml:mover><mml:msub><mml:mi>c</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>i</mml:mi></mml:mrow></mml:msub><mml:mo stretchy="false">^</mml:mo></mml:mover></mml:mrow></mml:mstyle></mml:math></inline-formula> is the probability assigned to the choice on trial <inline-formula><mml:math id="inf130"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>i</mml:mi></mml:mstyle></mml:math></inline-formula> obtained from the best-fitting logistic regression model.</p><p>We complemented this iterative algorithm with a second approach that estimates <inline-formula><mml:math id="inf131"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msup><mml:mi>δ</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mo>∗</mml:mo></mml:mrow></mml:msup></mml:mstyle></mml:math></inline-formula> using the history of choices preceding each trial. Nearly identical <inline-formula><mml:math id="inf132"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>δ</mml:mi></mml:mstyle></mml:math></inline-formula> values are derived using a single logistic regression model in which the binary choice made on each trial depends on the number of times each of the two items was selected and rejected on previous trials. The model is:<disp-formula id="equ14"><label>(14)</label><mml:math id="m14"><mml:mrow><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mrow><mml:mi mathvariant="normal">l</mml:mi><mml:mi mathvariant="normal">o</mml:mi><mml:mi mathvariant="normal">g</mml:mi><mml:mi mathvariant="normal">i</mml:mi><mml:mi mathvariant="normal">t</mml:mi></mml:mrow><mml:mo stretchy="false">[</mml:mo><mml:msub><mml:mi>p</mml:mi><mml:mrow><mml:mrow><mml:mi mathvariant="normal">r</mml:mi><mml:mi mathvariant="normal">i</mml:mi><mml:mi mathvariant="normal">g</mml:mi><mml:mi mathvariant="normal">h</mml:mi><mml:mi mathvariant="normal">t</mml:mi></mml:mrow></mml:mrow></mml:msub><mml:mo stretchy="false">]</mml:mo><mml:mo>=</mml:mo><mml:munderover><mml:mo>∑</mml:mo><mml:mrow><mml:mi>i</mml:mi><mml:mo>=</mml:mo><mml:mn>1</mml:mn></mml:mrow><mml:mrow><mml:msub><mml:mi>N</mml:mi><mml:mrow><mml:mrow><mml:mi mathvariant="normal">s</mml:mi><mml:mi mathvariant="normal">u</mml:mi><mml:mi mathvariant="normal">b</mml:mi><mml:mi mathvariant="normal">j</mml:mi></mml:mrow></mml:mrow></mml:msub></mml:mrow></mml:munderover><mml:msub><mml:mi>β</mml:mi><mml:mrow><mml:mn>0</mml:mn><mml:mo>,</mml:mo><mml:mi>i</mml:mi></mml:mrow></mml:msub><mml:msub><mml:mi>I</mml:mi><mml:mrow><mml:mi>i</mml:mi></mml:mrow></mml:msub><mml:mo>+</mml:mo><mml:munderover><mml:mo>∑</mml:mo><mml:mrow><mml:mi>i</mml:mi><mml:mo>=</mml:mo><mml:mn>1</mml:mn></mml:mrow><mml:mrow><mml:msub><mml:mi>N</mml:mi><mml:mrow><mml:mrow><mml:mi mathvariant="normal">s</mml:mi><mml:mi mathvariant="normal">u</mml:mi><mml:mi mathvariant="normal">b</mml:mi><mml:mi mathvariant="normal">j</mml:mi></mml:mrow></mml:mrow></mml:msub></mml:mrow></mml:munderover><mml:msub><mml:mi>β</mml:mi><mml:mrow><mml:mn>1</mml:mn><mml:mo>,</mml:mo><mml:mi>i</mml:mi></mml:mrow></mml:msub><mml:msub><mml:mi>I</mml:mi><mml:mrow><mml:mi>i</mml:mi></mml:mrow></mml:msub><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow><mml:mi>s</mml:mi></mml:mrow></mml:msub><mml:mo>+</mml:mo><mml:munderover><mml:mo>∑</mml:mo><mml:mrow><mml:mi>i</mml:mi><mml:mo>=</mml:mo><mml:mn>1</mml:mn></mml:mrow><mml:mrow><mml:msub><mml:mi>N</mml:mi><mml:mrow><mml:mrow><mml:mi mathvariant="normal">s</mml:mi><mml:mi mathvariant="normal">u</mml:mi><mml:mi mathvariant="normal">b</mml:mi><mml:mi mathvariant="normal">j</mml:mi></mml:mrow></mml:mrow></mml:msub></mml:mrow></mml:munderover><mml:msub><mml:mi>β</mml:mi><mml:mrow><mml:mn>2</mml:mn><mml:mo>,</mml:mo><mml:mi>i</mml:mi></mml:mrow></mml:msub><mml:msub><mml:mi>I</mml:mi><mml:mrow><mml:mi>i</mml:mi></mml:mrow></mml:msub><mml:msub><mml:mi mathvariant="normal">Δ</mml:mi><mml:mrow><mml:mi>c</mml:mi><mml:mi>h</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:mrow></mml:math></disp-formula></p><p>where, as before, <inline-formula><mml:math id="inf133"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msub><mml:mi>I</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>i</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula> is an indicator variable that takes a value of 1 if the trial was completed by subject <inline-formula><mml:math id="inf134"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>i</mml:mi></mml:mstyle></mml:math></inline-formula> and 0 otherwise. The key variable is <inline-formula><mml:math id="inf135"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msub><mml:mi mathvariant="normal">Δ</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>c</mml:mi><mml:mi>h</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula>. It depends on the number of past trials in which the item presented on the right in the current trial was chosen (<inline-formula><mml:math id="inf136"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msubsup><mml:mi>n</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi mathvariant="normal">c</mml:mi><mml:mi mathvariant="normal">h</mml:mi></mml:mrow></mml:mrow><mml:mrow class="MJX-TeXAtom-ORD"><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi mathvariant="normal">r</mml:mi><mml:mi mathvariant="normal">i</mml:mi><mml:mi mathvariant="normal">g</mml:mi><mml:mi mathvariant="normal">h</mml:mi><mml:mi mathvariant="normal">t</mml:mi></mml:mrow></mml:mrow></mml:msubsup></mml:mstyle></mml:math></inline-formula>) and not chosen (<inline-formula><mml:math id="inf137"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msubsup><mml:mi>n</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi mathvariant="normal">¬</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi mathvariant="normal">c</mml:mi><mml:mi mathvariant="normal">h</mml:mi></mml:mrow></mml:mrow><mml:mrow class="MJX-TeXAtom-ORD"><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi mathvariant="normal">r</mml:mi><mml:mi mathvariant="normal">i</mml:mi><mml:mi mathvariant="normal">g</mml:mi><mml:mi mathvariant="normal">h</mml:mi><mml:mi mathvariant="normal">t</mml:mi></mml:mrow></mml:mrow></mml:msubsup></mml:mstyle></mml:math></inline-formula>), and similarly, the number of past trials in which the item presented on the left in the current trial was chosen (<inline-formula><mml:math id="inf138"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msubsup><mml:mi>n</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi mathvariant="normal">c</mml:mi><mml:mi mathvariant="normal">h</mml:mi></mml:mrow></mml:mrow><mml:mrow class="MJX-TeXAtom-ORD"><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi mathvariant="normal">l</mml:mi><mml:mi mathvariant="normal">e</mml:mi><mml:mi mathvariant="normal">f</mml:mi><mml:mi mathvariant="normal">t</mml:mi></mml:mrow></mml:mrow></mml:msubsup></mml:mstyle></mml:math></inline-formula>) and not chosen (<inline-formula><mml:math id="inf139"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msubsup><mml:mi>n</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi mathvariant="normal">¬</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi mathvariant="normal">c</mml:mi><mml:mi mathvariant="normal">h</mml:mi></mml:mrow></mml:mrow><mml:mrow class="MJX-TeXAtom-ORD"><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi mathvariant="normal">l</mml:mi><mml:mi mathvariant="normal">e</mml:mi><mml:mi mathvariant="normal">f</mml:mi><mml:mi mathvariant="normal">t</mml:mi></mml:mrow></mml:mrow></mml:msubsup></mml:mstyle></mml:math></inline-formula>):<disp-formula id="equ15"><label>(15)</label><mml:math id="m15"><mml:mrow><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msub><mml:mi mathvariant="normal">Δ</mml:mi><mml:mrow><mml:mi>c</mml:mi><mml:mi>h</mml:mi></mml:mrow></mml:msub><mml:mo>=</mml:mo><mml:msubsup><mml:mi>n</mml:mi><mml:mrow><mml:mrow><mml:mi mathvariant="normal">c</mml:mi><mml:mi mathvariant="normal">h</mml:mi></mml:mrow></mml:mrow><mml:mrow><mml:mrow><mml:mi mathvariant="normal">r</mml:mi><mml:mi mathvariant="normal">i</mml:mi><mml:mi mathvariant="normal">g</mml:mi><mml:mi mathvariant="normal">h</mml:mi><mml:mi mathvariant="normal">t</mml:mi></mml:mrow></mml:mrow></mml:msubsup><mml:mo>−</mml:mo><mml:msubsup><mml:mi>n</mml:mi><mml:mrow><mml:mi mathvariant="normal">¬</mml:mi><mml:mrow><mml:mi mathvariant="normal">c</mml:mi><mml:mi mathvariant="normal">h</mml:mi></mml:mrow></mml:mrow><mml:mrow><mml:mrow><mml:mi mathvariant="normal">r</mml:mi><mml:mi mathvariant="normal">i</mml:mi><mml:mi mathvariant="normal">g</mml:mi><mml:mi mathvariant="normal">h</mml:mi><mml:mi mathvariant="normal">t</mml:mi></mml:mrow></mml:mrow></mml:msubsup><mml:mo>+</mml:mo><mml:msubsup><mml:mi>n</mml:mi><mml:mrow><mml:mi mathvariant="normal">¬</mml:mi><mml:mrow><mml:mi mathvariant="normal">c</mml:mi><mml:mi mathvariant="normal">h</mml:mi></mml:mrow></mml:mrow><mml:mrow><mml:mrow><mml:mi mathvariant="normal">l</mml:mi><mml:mi mathvariant="normal">e</mml:mi><mml:mi mathvariant="normal">f</mml:mi><mml:mi mathvariant="normal">t</mml:mi></mml:mrow></mml:mrow></mml:msubsup><mml:mo>−</mml:mo><mml:msubsup><mml:mi>n</mml:mi><mml:mrow><mml:mrow><mml:mi mathvariant="normal">c</mml:mi><mml:mi mathvariant="normal">h</mml:mi></mml:mrow></mml:mrow><mml:mrow><mml:mrow><mml:mi mathvariant="normal">l</mml:mi><mml:mi mathvariant="normal">e</mml:mi><mml:mi mathvariant="normal">f</mml:mi><mml:mi mathvariant="normal">t</mml:mi></mml:mrow></mml:mrow></mml:msubsup><mml:mo>.</mml:mo></mml:mstyle></mml:mrow></mml:math></disp-formula></p><p>The variable <inline-formula><mml:math id="inf140"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msub><mml:mi mathvariant="normal">Δ</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>c</mml:mi><mml:mi>h</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula> represents the influence of past choices. The signs in <xref ref-type="disp-formula" rid="equ15">Equation 15</xref> are such that a positive (negative) value of <inline-formula><mml:math id="inf141"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msub><mml:mi mathvariant="normal">Δ</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>c</mml:mi><mml:mi>h</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula> indicates a bias toward the right (left) item. To obtain the <inline-formula><mml:math id="inf142"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msup><mml:mi>δ</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mo>∗</mml:mo></mml:mrow></mml:msup></mml:mstyle></mml:math></inline-formula> in units equivalent to those derived with <italic>Reval</italic>, we need to divide the regression coefficient <inline-formula><mml:math id="inf143"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msub><mml:mi>β</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mn>2</mml:mn><mml:mo>,</mml:mo><mml:mi>i</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula> by the sensitivity coefficient <inline-formula><mml:math id="inf144"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msub><mml:mi>β</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mn>1</mml:mn><mml:mo>,</mml:mo><mml:mi>i</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula>, separately for each subject <inline-formula><mml:math id="inf145"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>i</mml:mi></mml:mstyle></mml:math></inline-formula>. As can be seen in <xref ref-type="fig" rid="fig5s3">Figure 5—figure supplement 3</xref>, the values obtained with this method are almost identical to those obtained with the <italic>Reval</italic> algorithm.</p></sec><sec id="s4-5"><title>Correlated-evidence DDM</title><p>The model assumes that at each moment during the decision-making process, the decision-maker can only access a noisy sample of the value of each item. These samples are normally distributed, with parameters such that their unbounded accumulation over one second is also normally distributed with a mean equal to <inline-formula><mml:math id="inf146"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>κ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>s</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula>, where <inline-formula><mml:math id="inf147"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msub><mml:mi>v</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>s</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula> is the explicit value reported during the Ratings phase and <inline-formula><mml:math id="inf148"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>κ</mml:mi></mml:mstyle></mml:math></inline-formula> is a measure of signal-to-noise, and a standard deviation equal to 1.</p><p>Crucially, for each item, the noise in successive samples is correlated. To generate the correlated samples, we sample from a Markov chain using the Metropolis-Hastings algorithm (<xref ref-type="bibr" rid="bib17">Chib and Greenberg, 1995</xref>). The target distribution is the normally distributed value function described in the previous paragraph. The proposal density is also normally distributed. Its width determines the degree of correlation between consecutive samples. Typically, the correlation between successive samples is considered a limitation of the Metropolis-Hastings algorithm. Here, however, it allows us to generate correlated samples from a target distribution. The standard deviation of the proposal density is <inline-formula><mml:math id="inf149"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msqrt><mml:mi>d</mml:mi><mml:mi>t</mml:mi></mml:msqrt><mml:mrow class="MJX-TeXAtom-ORD"><mml:mo>/</mml:mo></mml:mrow><mml:mi>τ</mml:mi></mml:mstyle></mml:math></inline-formula>. Higher values of <inline-formula><mml:math id="inf150"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>τ</mml:mi></mml:mstyle></mml:math></inline-formula> result in a narrower proposal density, hence more strongly correlated samples. We sample from the same Markov chain across different trials in which the same item is presented, so that the last sample obtained about an item in a given trial is the initial state of the Markov chain the next time the item is presented.</p><p>At each moment (<inline-formula><mml:math id="inf151"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>d</mml:mi><mml:mi>t</mml:mi><mml:mo>=</mml:mo><mml:mn>40</mml:mn><mml:mi>m</mml:mi><mml:mi>s</mml:mi></mml:mstyle></mml:math></inline-formula>), we sample one value for the left item and another for the right item, compute their difference (right minus left), and accumulate this difference until it crosses a threshold at <inline-formula><mml:math id="inf152"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mo>+</mml:mo><mml:msub><mml:mi>B</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mn>0</mml:mn></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula>, signaling a rightward choice, or at <inline-formula><mml:math id="inf153"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mo>−</mml:mo><mml:msub><mml:mi>B</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mn>0</mml:mn></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula>, signaling a leftward choice. The decision time is added to the non-decision time, <inline-formula><mml:math id="inf154"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msub><mml:mi>μ</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>n</mml:mi><mml:mi>d</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula>, to obtain the response time.</p><p>We fit the model to the data as follows. For each item, we simulate many Markov chains. In each trial, <inline-formula><mml:math id="inf155"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>i</mml:mi></mml:mstyle></mml:math></inline-formula>, we take samples from each chain until the accumulation of these samples reaches one of the two decision thresholds. Then we calculate the likelihood (<inline-formula><mml:math id="inf156"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>L</mml:mi></mml:mstyle></mml:math></inline-formula>) of obtaining the choice and the RT displayed by the participant on that trial as:<disp-formula id="equ16"><label>(16)</label><mml:math id="m16"><mml:mrow><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mtable columnalign="right left right left right left right left right left right left" rowspacing="3pt" columnspacing="0em 2em 0em 2em 0em 2em 0em 2em 0em 2em 0em" displaystyle="true"><mml:mtr><mml:mtd><mml:mi>L</mml:mi><mml:mo stretchy="false">(</mml:mo><mml:mrow><mml:mi mathvariant="normal">c</mml:mi><mml:mi mathvariant="normal">h</mml:mi><mml:mi mathvariant="normal">o</mml:mi><mml:mi mathvariant="normal">i</mml:mi><mml:mi mathvariant="normal">c</mml:mi><mml:msub><mml:mi mathvariant="normal">e</mml:mi><mml:mi mathvariant="normal">i</mml:mi></mml:msub><mml:mo>,</mml:mo><mml:mi mathvariant="normal">R</mml:mi><mml:msub><mml:mi mathvariant="normal">T</mml:mi><mml:mi mathvariant="normal">i</mml:mi></mml:msub></mml:mrow><mml:mo stretchy="false">)</mml:mo></mml:mtd><mml:mtd><mml:mi/><mml:mo>=</mml:mo><mml:mfrac><mml:mn>1</mml:mn><mml:mi>N</mml:mi></mml:mfrac><mml:munderover><mml:mo>∑</mml:mo><mml:mrow><mml:mi>j</mml:mi><mml:mo>=</mml:mo><mml:mn>1</mml:mn></mml:mrow><mml:mrow><mml:mi>N</mml:mi></mml:mrow></mml:munderover><mml:msub><mml:mi>L</mml:mi><mml:mrow><mml:mi>j</mml:mi></mml:mrow></mml:msub><mml:mo stretchy="false">(</mml:mo><mml:mrow><mml:mi mathvariant="normal">c</mml:mi><mml:mi mathvariant="normal">h</mml:mi><mml:mi mathvariant="normal">o</mml:mi><mml:mi mathvariant="normal">i</mml:mi><mml:mi mathvariant="normal">c</mml:mi><mml:msub><mml:mi mathvariant="normal">e</mml:mi><mml:mi mathvariant="normal">i</mml:mi></mml:msub><mml:mo>,</mml:mo><mml:mi mathvariant="normal">R</mml:mi><mml:msub><mml:mi mathvariant="normal">T</mml:mi><mml:mi mathvariant="normal">i</mml:mi></mml:msub></mml:mrow><mml:mo stretchy="false">)</mml:mo></mml:mtd></mml:mtr><mml:mtr><mml:mtd><mml:msub><mml:mi>L</mml:mi><mml:mrow><mml:mi>j</mml:mi></mml:mrow></mml:msub><mml:mo stretchy="false">(</mml:mo><mml:mrow><mml:mi mathvariant="normal">c</mml:mi><mml:mi mathvariant="normal">h</mml:mi><mml:mi mathvariant="normal">o</mml:mi><mml:mi mathvariant="normal">i</mml:mi><mml:mi mathvariant="normal">c</mml:mi><mml:msub><mml:mi mathvariant="normal">e</mml:mi><mml:mi mathvariant="normal">i</mml:mi></mml:msub><mml:mo>,</mml:mo><mml:mi mathvariant="normal">R</mml:mi><mml:msub><mml:mi mathvariant="normal">T</mml:mi><mml:mi mathvariant="normal">i</mml:mi></mml:msub></mml:mrow><mml:mo stretchy="false">)</mml:mo></mml:mtd><mml:mtd><mml:mi/><mml:mo>=</mml:mo><mml:msub><mml:mrow><mml:mn mathvariant="double-struck">1</mml:mn></mml:mrow><mml:mrow><mml:mi>i</mml:mi><mml:mo>,</mml:mo><mml:mi>j</mml:mi></mml:mrow></mml:msub><mml:mspace width="thinmathspace"/><mml:mrow><mml:mi class="mathcal" mathvariant="script">N</mml:mi></mml:mrow><mml:mo stretchy="false">(</mml:mo><mml:mrow><mml:mi mathvariant="normal">R</mml:mi><mml:msub><mml:mi mathvariant="normal">T</mml:mi><mml:mi mathvariant="normal">i</mml:mi></mml:msub></mml:mrow><mml:mrow><mml:mo stretchy="false">|</mml:mo></mml:mrow><mml:mrow><mml:mi mathvariant="normal">R</mml:mi><mml:msubsup><mml:mi mathvariant="normal">T</mml:mi><mml:mi mathvariant="normal">i</mml:mi><mml:mrow><mml:mo stretchy="false">(</mml:mo><mml:mi mathvariant="normal">j</mml:mi><mml:mo stretchy="false">)</mml:mo></mml:mrow></mml:msubsup><mml:mo>,</mml:mo><mml:msub><mml:mi>σ</mml:mi><mml:mrow><mml:mi mathvariant="normal">n</mml:mi><mml:mi mathvariant="normal">d</mml:mi></mml:mrow></mml:msub></mml:mrow><mml:mo stretchy="false">)</mml:mo></mml:mtd></mml:mtr></mml:mtable></mml:mstyle></mml:mrow></mml:math></disp-formula></p><p>where <inline-formula><mml:math id="inf157"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>N</mml:mi><mml:mo>=</mml:mo><mml:mn>1</mml:mn><mml:mo>,</mml:mo><mml:mn>000</mml:mn></mml:mstyle></mml:math></inline-formula> is the number of Markov chains, <inline-formula><mml:math id="inf158"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mrow><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msub><mml:mrow><mml:mn mathvariant="double-struck">1</mml:mn></mml:mrow><mml:mrow><mml:mi>i</mml:mi><mml:mo>,</mml:mo><mml:mi>j</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:mrow></mml:mstyle></mml:math></inline-formula> is an indicator function that takes the value 1 if the choice made on chain <inline-formula><mml:math id="inf159"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>j</mml:mi></mml:mstyle></mml:math></inline-formula> is the same as the choice made by the participant on trial <inline-formula><mml:math id="inf160"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>i</mml:mi></mml:mstyle></mml:math></inline-formula> and 0 otherwise, <inline-formula><mml:math id="inf161"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi class="MJX-tex-caligraphic" mathvariant="script">N</mml:mi></mml:mrow><mml:mo stretchy="false">(</mml:mo><mml:mi>x</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mo stretchy="false">|</mml:mo></mml:mrow><mml:mi>y</mml:mi><mml:mo>,</mml:mo><mml:mi>z</mml:mi><mml:mo stretchy="false">)</mml:mo></mml:mstyle></mml:math></inline-formula> is the normal probability density function with mean <inline-formula><mml:math id="inf162"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>y</mml:mi></mml:mstyle></mml:math></inline-formula> and standard deviation <inline-formula><mml:math id="inf163"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>z</mml:mi></mml:mstyle></mml:math></inline-formula> evaluated at <inline-formula><mml:math id="inf164"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>x</mml:mi></mml:mstyle></mml:math></inline-formula>, and <inline-formula><mml:math id="inf165"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msub><mml:mi>σ</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>n</mml:mi><mml:mi>d</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula> is a parameter fit to the data.</p><p>When an item is presented again in a future trial, the initial state of each Markov chain depends on the state it was in the last time the item was presented. The initial state of each chain is obtained by sampling 1000 values (one per chain) from the distribution given by the final state of each chain. The sampling is weighted by the value of <inline-formula><mml:math id="inf166"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msub><mml:mi>L</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>j</mml:mi></mml:mrow></mml:msub></mml:mstyle></mml:math></inline-formula> of each chain (<xref ref-type="disp-formula" rid="equ16">Equation 16</xref>), so that chains that better explained the choice and RT in the last trial are more likely to be sampled from in future trials.</p><p>The model has 5 parameters per participant: <inline-formula><mml:math id="inf167"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mo fence="false" stretchy="false">{</mml:mo><mml:mi>κ</mml:mi><mml:mo>,</mml:mo><mml:msub><mml:mi>B</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mn>0</mml:mn></mml:mrow></mml:msub><mml:mo>,</mml:mo><mml:mi>τ</mml:mi><mml:mo>,</mml:mo><mml:msub><mml:mi>μ</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>n</mml:mi><mml:mi>d</mml:mi></mml:mrow></mml:msub><mml:mo>,</mml:mo><mml:msub><mml:mi>σ</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>n</mml:mi><mml:mi>d</mml:mi></mml:mrow></mml:msub><mml:mo fence="false" stretchy="false">}</mml:mo></mml:mstyle></mml:math></inline-formula>, which were fit to maximize the sum, across trials, of the log of <inline-formula><mml:math id="inf168"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>L</mml:mi></mml:mstyle></mml:math></inline-formula> using BADS (<xref ref-type="bibr" rid="bib3">Acerbi and Ma, 2017</xref>).</p><p>The correlations in <xref ref-type="fig" rid="fig11">Figure 11B</xref> were generated using the best-fitting parameters for each participant to simulate 100,000 Markov chains. We generate Markov chain samples independently for the left and right items over a 1 s period. To illustrate noise correlations, the simulations assume that the static value of both the left and right items is zero. We then calculate the difference in dynamic value (<inline-formula><mml:math id="inf169"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>x</mml:mi></mml:mstyle></mml:math></inline-formula>) between the left and right items at each time (<inline-formula><mml:math id="inf170"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>t</mml:mi></mml:mstyle></mml:math></inline-formula>) and for each of the Markov chains (<inline-formula><mml:math id="inf171"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>i</mml:mi></mml:mstyle></mml:math></inline-formula>). Pearson’s correlation is computed between these differences at time zero, <inline-formula><mml:math id="inf172"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msub><mml:mi>x</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>i</mml:mi></mml:mrow></mml:msub><mml:mo stretchy="false">(</mml:mo><mml:mi>t</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mo>=</mml:mo></mml:mrow><mml:mn>0</mml:mn><mml:mo stretchy="false">)</mml:mo></mml:mstyle></mml:math></inline-formula>, and at time <inline-formula><mml:math id="inf173"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:msub><mml:mi>x</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mi>i</mml:mi></mml:mrow></mml:msub><mml:mo stretchy="false">(</mml:mo><mml:mi>t</mml:mi><mml:mrow class="MJX-TeXAtom-ORD"><mml:mo>=</mml:mo></mml:mrow><mml:mi>τ</mml:mi><mml:mo stretchy="false">)</mml:mo></mml:mstyle></mml:math></inline-formula>, for different time lags <inline-formula><mml:math id="inf174"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mi>τ</mml:mi></mml:mstyle></mml:math></inline-formula>. Correlations were calculated independently for each participant. Each trace in <xref ref-type="fig" rid="fig11">Figure 11B</xref> represents a different participant.</p></sec><sec id="s4-6"><title>fMRI analysis</title><sec id="s4-6-1"><title>Acquisition</title><p>Imaging data were acquired on a 3T GE MR750 MRI scanner with a 32-channel head coil. Functional data were acquired using a T2*-weighted echo planar imaging sequence (repetition time (TR)=2 s, echo time (TE)=22ms, flip angle (FA) = 70°, field of view (FOV)=192 mm, acquisition matrix of 96x96). Forty oblique axial slices were acquired with a 2 mm in-plane resolution positioned along the anterior commissure-posterior commissure line and spaced 3 mm to achieve full brain coverage. Slices were acquired in an interleaved fashion. We acquired three runs of the food choice task, each composed of 70 trials. Each of the food choice task functional runs consisted of 212 volumes and lasted 7 min. In addition to functional data, a single three-dimensional high-resolution (1 mm isotropic) T1-weighted full-brain image was acquired using a BRAVO pulse sequence for brain masking and image registration.</p></sec><sec id="s4-6-2"><title>Preprocessing</title><p>Raw DICOM files were converted into Nifti file format and organized in the Brain Imaging Data Structure (BIDS) using dcm2niix (<xref ref-type="bibr" rid="bib48">Li et al., 2016</xref>). Results included in this manuscript come from preprocessing performed using <italic>fMRIPrep</italic> 22.1.1 (<xref ref-type="bibr" rid="bib22">Esteban et al., 2019</xref>; <xref ref-type="bibr" rid="bib21">Esteban et al., 2018</xref>; RRID:<ext-link ext-link-type="uri" xlink:href="https://identifiers.org/RRID/RRID:SCR_016216">SCR_016216</ext-link>), which is based on <italic>Nipype</italic> 1.8.5 (<xref ref-type="bibr" rid="bib27">Gorgolewski et al., 2011</xref>; <xref ref-type="bibr" rid="bib28">Gorgolewski et al., 2018</xref>; RRID:<ext-link ext-link-type="uri" xlink:href="https://identifiers.org/RRID/RRID:SCR_002502">SCR_002502</ext-link>).</p></sec><sec id="s4-6-3"><title>Anatomical data preprocessing</title><p>The T1-weighted (T1w) image was corrected for intensity non-uniformity (INU) with <monospace>N4BiasFieldCorrection</monospace> (<xref ref-type="bibr" rid="bib70">Tustison et al., 2010</xref>), distributed with ANTs 2.3.3 (<xref ref-type="bibr" rid="bib4">Avants et al., 2008</xref>, RRID:<ext-link ext-link-type="uri" xlink:href="https://identifiers.org/RRID/RRID:SCR_004757">SCR_004757</ext-link>), and used as T1w-reference throughout the workflow. The T1w-reference was then skull-stripped with a <italic>Nipype</italic> implementation of the <monospace>antsBrainExtraction.sh</monospace> workflow (from ANTs), using OASIS30ANTs as target template. Volume-based spatial normalization to one standard space (MNI152NLin2009cAsym) was performed through nonlinear registration with <monospace>antsRegistration</monospace> (ANTs 2.3.3), using brain-extracted versions of both T1w reference and the T1w template. The following template was selected for spatial normalization: <italic>ICBM 152 Nonlinear Asymmetrical template version 2009c</italic> [<xref ref-type="bibr" rid="bib25">Fonov et al., 2009</xref>, RRID:<ext-link ext-link-type="uri" xlink:href="https://identifiers.org/RRID/RRID:SCR_008796">SCR_008796</ext-link>; TemplateFlow ID: MNI152NLin2009cAsym].</p></sec><sec id="s4-6-4"><title>Functional data preprocessing</title><p>For each of the three BOLD runs per subject, the following preprocessing was performed. First, a reference volume and its skull-stripped version were generated using a custom methodology of <italic>fMRIPrep</italic>. Head-motion parameters with respect to the BOLD reference (transformation matrices, and six corresponding rotation and translation parameters) are estimated before any spatiotemporal filtering using <monospace>mcflirt</monospace> (FSL 6.0.5.1:57b01774, <xref ref-type="bibr" rid="bib34">Jenkinson et al., 2002</xref>). The BOLD time-series (including slice-timing correction when applied) were resampled onto their original, native space by applying the transforms to correct for head-motion. These resampled BOLD time-series will be referred to as <italic>preprocessed BOLD in original space</italic>, or just <italic>preprocessed BOLD</italic>. The BOLD reference was then co-registered to the T1w reference using <monospace>mri_coreg</monospace> (FreeSurfer) followed by <monospace>flirt</monospace> (FSL 6.0.5.1:57b01774, <xref ref-type="bibr" rid="bib33">Jenkinson and Smith, 2001</xref>) with the boundary-based registration (<xref ref-type="bibr" rid="bib29">Greve and Fischl, 2009</xref>) cost-function. Co-registration was configured with six degrees of freedom. Several confounding time-series were calculated based on the <italic>preprocessed BOLD</italic>: framewise displacement (FD) and DVARS. FD was computed using two formulations following Power (absolute sum of relative motions, <xref ref-type="bibr" rid="bib57">Power et al., 2014</xref>) and Jenkinson (relative root mean square displacement between affines, <xref ref-type="bibr" rid="bib34">Jenkinson et al., 2002</xref>). FD and DVARS are calculated for each functional run, both using their implementations in <italic>Nipype</italic> (following the definitions by <xref ref-type="bibr" rid="bib57">Power et al., 2014</xref>). The head-motion estimates calculated in the correction step were also placed within the corresponding confounds file. The confound time series were derived from head motion estimates (<xref ref-type="bibr" rid="bib62">Satterthwaite et al., 2013</xref>). Frames that exceeded a threshold of 0.5 mm FD or 1.5 standardized DVARS were annotated as motion outliers. The BOLD time-series were resampled into standard space, generating a <italic>preprocessed BOLD run in MNI152NLin2009cAsym space</italic>. First, a reference volume and its skull-stripped version were generated using a custom methodology of <italic>fMRIPrep</italic>. All resamplings can be performed with <italic>a single interpolation step</italic> by composing all the pertinent transformations (i.e. head-motion transform matrices, susceptibility distortion correction when available, and co-registrations to anatomical and output spaces). Gridded (volumetric) resamplings were performed using antsApplyTransforms (ANTs), configured with Lanczos interpolation to minimize the smoothing effects of other kernels (<xref ref-type="bibr" rid="bib45">Lanczos, 1964</xref>).</p><p>Many internal operations of <italic>fMRIPrep</italic> use <italic>Nilearn</italic> 0.9.1 (<xref ref-type="bibr" rid="bib1">Abraham et al., 2014</xref>, RRID:<ext-link ext-link-type="uri" xlink:href="https://identifiers.org/RRID/RRID:SCR_001362">SCR_001362</ext-link>), mostly within the functional processing workflow. For more details of the pipeline, see <ext-link ext-link-type="uri" xlink:href="https://fmriprep.readthedocs.io/en/latest/workflows.html">the section corresponding to workflows in fMRIPrep’s documentation</ext-link>.</p></sec><sec id="s4-6-5"><title>Analysis</title><p>We conducted a GLM analysis to look at BOLD activity related to <italic>d-values</italic>, <italic>s-values</italic>, and the difference between the two. We ran four separate models.</p><p><italic>Main fMRI Model</italic> included five regressors: (<italic>i</italic>) onsets for all valid trials, modeled with a duration equal to the average RT across all valid choices and participants; (<italic>ii</italic>) same onsets and duration as (<italic>i</italic>) modulated by RT demeaned across these trials within each run for each participant; (<italic>iii</italic>) same onsets and duration as (<italic>i</italic>) but modulated by the <italic>s-value</italic> of the chosen item demeaned across trials within each run for each participant; (<italic>iv</italic>) same onsets and duration as (<italic>i</italic>) but modulated by the <italic>d-value</italic> of the chosen item demeaned across these trials within each run for each participant; (<italic>v</italic>) onsets for missed trials. The map in <xref ref-type="fig" rid="fig9">Figure 9</xref> was generated using this model.</p><p>fMRI Model of s-value only included four regressors; all but regressor (<italic>iv</italic>) in <italic>Main fMRI Model</italic>. The map in <xref ref-type="fig" rid="fig9s1">Figure 9—figure supplement 1</xref> top was generated using this model.</p><p>fMRI model of d-value only included four regressors; all but regressor (<italic>iii</italic>) in <italic>Main fMRI Model</italic>. The map in <xref ref-type="fig" rid="fig9s1">Figure 9—figure supplement 1</xref> middle was generated using this model.</p><p>fMRI model of d-value s-value only included four regressors; regressors (<italic>i</italic>) and (<italic>ii</italic>) were the same as in <italic>Main fMRI Model</italic>, regressor (<italic>iii</italic>) had the same onsets and duration as (<italic>i</italic>) but modulated by (<italic>d-value</italic><inline-formula><mml:math id="inf175"><mml:mstyle displaystyle="true" scriptlevel="0"><mml:mo>−</mml:mo></mml:mstyle></mml:math></inline-formula><italic>s-value</italic>) of the chosen item demeaned across trials within each run for each participant, and regressor (<italic>iv</italic>) included onsets for missed trials. The map in <xref ref-type="fig" rid="fig9s1">Figure 9—figure supplement 1</xref> bottom was generated using this model.</p><p>All four models included the six x, y, z translation and rotation motion parameters, FD, DVARS, and motion outliers obtained from textitfmriprep (described above) as confound regressors of no interest. All regressors were entered at the first level of analysis, and all (except the added confound regressors) were convolved with a canonical double-gamma hemodynamic response function. The time derivative of each regressor (except the added confounding regressors) was included in the model. No orthogonalization between regressors was performed. Models were estimated separately for each participant and run.</p><p>GLMs were estimated using FSL’s FMRI Expert Analysis Tool (FEAT). The first-level time-series GLM analysis was performed for each run per participant using FSL’s FILM. The first-level contrast images were then combined across runs per participant using fixed effects. The group-level analysis was performed using FMRIB’s Local Analysis of Mixed Effects (FLAME1; <xref ref-type="bibr" rid="bib7">Beckmann et al., 2003</xref>). Group-level maps were corrected to control the family-wise error rate using cluster-based Gaussian random field correction for multiple comparisons, with an uncorrected cluster-forming threshold of z=3.1 and corrected extent threshold of p&lt;0.05.</p></sec></sec></sec></body><back><sec sec-type="additional-information" id="s5"><title>Additional information</title><fn-group content-type="competing-interest"><title>Competing interests</title><fn fn-type="COI-statement" id="conf1"><p>No competing interests declared</p></fn></fn-group><fn-group content-type="author-contribution"><title>Author contributions</title><fn fn-type="con" id="con1"><p>Conceptualization, Data curation, Software, Formal analysis, Validation, Investigation, Visualization, Methodology, Writing – original draft, Writing – review and editing</p></fn><fn fn-type="con" id="con2"><p>Data curation, Software, Formal analysis, Validation, Investigation, Visualization, Methodology, Writing – review and editing</p></fn><fn fn-type="con" id="con3"><p>Resources, Supervision, Funding acquisition, Project administration, Writing – review and editing</p></fn><fn fn-type="con" id="con4"><p>Resources, Supervision, Funding acquisition, Project administration, Writing – review and editing</p></fn></fn-group></sec><sec sec-type="supplementary-material" id="s6"><title>Additional files</title><supplementary-material id="mdar"><label>MDAR checklist</label><media xlink:href="elife-96997-mdarchecklist1-v1.pdf" mimetype="application" mime-subtype="pdf"/></supplementary-material><supplementary-material id="supp1"><label>Supplementary file 1.</label><caption><title>Activation table for map in <xref ref-type="fig" rid="fig9">Figure 9</xref>.</title><p>The effect of d-value on BOLD in Main fMRI model. For each cluster, the list shows regions from the Harvard-Oxford atlas that contained a peak activation of a subcluster, along with the peak p-value, the peak effect size, and the peak X/Y/Z location for the cluster in MNI space.</p></caption><media xlink:href="elife-96997-supp1-v1.pdf" mimetype="application" mime-subtype="pdf"/></supplementary-material><supplementary-material id="supp2"><label>Supplementary file 2.</label><caption><title>Activation tables for maps in <xref ref-type="fig" rid="fig9s1">Figure 9—figure supplement 1</xref>.</title><p>The effect of s-value on BOLD in fMRI Model of s-value only (top), the effect of d-value on BOLD in fMRI Model of d-value only (middle), and the effect of (s-value − d-value) in fMRI model of (d-value − s-value) only (bottom). For each cluster, the list shows regions from the Harvard-Oxford atlas that contained a peak activation of a subcluster, along with the peak p-value, the peak effect size, and the peak X/Y/Z location for the cluster in MNI space.</p></caption><media xlink:href="elife-96997-supp2-v1.pdf" mimetype="application" mime-subtype="pdf"/></supplementary-material></sec><sec sec-type="data-availability" id="s7"><title>Data availability</title><p>The data and code required to reproduce the analyses and figures are available on <ext-link ext-link-type="uri" xlink:href="https://github.com/arielzylberberg/Reval_eLife_2024">GitHub</ext-link>, (copy archived at <xref ref-type="bibr" rid="bib80">Zylberberg, 2024</xref>).</p></sec><ack id="ack"><title>Acknowledgements</title><p>We thank Ari Pakman for helpful discussions.</p><p>This work was supported by the National Institutes of Health (R01NS113113 to MNS and MH121093 to DS), the Air Force Office of Scientific Research under award (FA9550-22-1-0337 to 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kwd-group-type="evidence-strength"><kwd>Convincing</kwd></kwd-group><kwd-group kwd-group-type="claim-importance"><kwd>Important</kwd></kwd-group></front-stub><body><p>This <bold>important</bold> study addresses key assumptions underlying current models of the formation of value-based decisions. The authors provide <bold>convincing</bold> evidence that the subjective values human participants assign to items change across sequences of multiple decisions. They establish methods to detect these changes in frequently used behavioral task designs.</p></body></sub-article><sub-article article-type="referee-report" id="sa1"><front-stub><article-id pub-id-type="doi">10.7554/eLife.96997.3.sa1</article-id><title-group><article-title>Reviewer #1 (Public review):</article-title></title-group><contrib-group><contrib contrib-type="author"><anonymous/><role specific-use="referee">Reviewer</role></contrib></contrib-group></front-stub><body><p>Summary:</p><p>There is a long-standing idea that choices influence evaluation: options we choose are re-evaluated to be better than they were before the choice. There has been some debate about this finding, and the authors developed several novel methods for detecting these re-evaluations in task designs where options are repeatedly presented against several alternatives. Using these novel methods the authors clearly demonstrate this re-evaluation phenomenon in several existing datasets and show that estimations of dynamic valuation correlate with neural activity in prefrontal cortex.</p><p>Strengths:</p><p>The paper is well-written and figures are clear. The authors provided evidence for the behaviour effect using several techniques and generated surrogate data (where the ground truth is known) to demonstrate the robustness of their methods. The author avoid over-selling the work, with a lucid description of limitations, and potential for further exploration of the work, in the discussion.</p><p>Comments on revisions:</p><p>The authors did a good job responding to the comments.</p></body></sub-article><sub-article article-type="referee-report" id="sa2"><front-stub><article-id pub-id-type="doi">10.7554/eLife.96997.3.sa2</article-id><title-group><article-title>Reviewer #2 (Public review):</article-title></title-group><contrib-group><contrib contrib-type="author"><anonymous/><role specific-use="referee">Reviewer</role></contrib></contrib-group></front-stub><body><p>Zylberberg and colleagues show that food choice outcomes and BOLD signal in the vmPFC are better explained by algorithms that update subjective values during the sequence of choices compared to algorithms based on static values acquired before the decision phase. This study presents a valuable means of reducing the apparent stochasticity of choices in common laboratory experiment designs. The evidence supporting the claims of the authors is solid, although currently limited to choices between food items because no other goods were examined. The work will be of interest to researchers examining decision making across various social and biological sciences.</p><p>Comments on revisions:</p><p>We thank the authors for carefully addressing our concerns about the first version of the manuscript. The manuscript text and contributions are now much more clear and convincing.</p></body></sub-article><sub-article article-type="author-comment" id="sa3"><front-stub><article-id pub-id-type="doi">10.7554/eLife.96997.3.sa3</article-id><title-group><article-title>Author response</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Zylberberg</surname><given-names>Ariel</given-names></name><role specific-use="author">Author</role><aff><institution>Columbia University</institution><addr-line><named-content content-type="city">New York</named-content></addr-line><country>United States</country></aff></contrib><contrib contrib-type="author"><name><surname>Bakkour</surname><given-names>Akram</given-names></name><role specific-use="author">Author</role><aff><institution>University of Chicago</institution><addr-line><named-content content-type="city">Illinois</named-content></addr-line><country>United States</country></aff></contrib><contrib contrib-type="author"><name><surname>Shohamy</surname><given-names>Daphna</given-names></name><role specific-use="author">Author</role><aff><institution>Columbia University</institution><addr-line><named-content content-type="city">New York</named-content></addr-line><country>United States</country></aff></contrib><contrib contrib-type="author"><name><surname>Shadlen</surname><given-names>Michael N</given-names></name><role specific-use="author">Author</role><aff><institution>Columbia University</institution><addr-line><named-content content-type="city">New York</named-content></addr-line><country>United States</country></aff></contrib></contrib-group></front-stub><body><p>The following is the authors’ response to the original reviews.</p><disp-quote content-type="editor-comment"><p><bold>Public Reviews:</bold></p><p><bold>Reviewer #1 (Public Review):</bold></p><p>Summary:</p><p>There is a long-standing idea that choices influence evaluation: options we choose are re-evaluated to be better than they were before the choice. There has been some debate about this finding, and the authors developed several novel methods for detecting these re-evaluations in task designs where options are repeatedly presented against several alternatives. Using these novel methods the authors clearly demonstrate this re-evaluation phenomenon in several existing datasets.</p><p>Strengths:</p><p>The paper is well-written and the figures are clear. The authors provided evidence for the behaviour effect using several techniques and generated surrogate data (where the ground truth is known) to demonstrate the robustness of their methods.</p><p>Weaknesses:</p><p>The description of the results of the fMRI analysis in the text is not complete: weakening the claim that their re-evaluation algorithm better reveals neural valuation processes.</p></disp-quote><p>We appreciate the reviewer’s comment regarding the incomplete account of the fMRI results. In response, we implemented Reviewer #2's suggestion to run additional GLM models for a clearer interpretation of our findings. We also took this opportunity to apply updated preprocessing to the fMRI data and revise the GLM models, making them both simpler and more comprehensive. The results section is thus substantially revised, now including a new main figure and several supplemental figures that more clearly present our fMRI findings. Additionally, we have uploaded the statistical maps to NeuroVault, allowing readers to explore the full maps interactively rather than relying solely on the static images in the paper. The new analyses strengthen our original conclusion: dynamic values (previously referred to as revalued values, following the reviewer’s suggestion) better explain BOLD activity in the ventromedial prefrontal cortex, a region consistently associated with valuation, than static values (values reported prior to the choice phase in the auction procedure).</p><disp-quote content-type="editor-comment"><p><bold>Reviewer #2 (Public Review):</bold></p><p>Summary:</p><p>Zylberberg and colleagues show that food choice outcomes and BOLD signal in the vmPFC are better explained by algorithms that update subjective values during the sequence of choices compared to algorithms based on static values acquired before the decision phase. This study presents a valuable means of reducing the apparent stochasticity of choices in common laboratory experiment designs. The evidence supporting the claims of the authors is solid, although currently limited to choices between food items because no other goods were examined. The work will be of interest to researchers examining decision-making across various social and biological sciences.</p><p>Strengths:</p><p>The paper analyses multiple food choice datasets to check the robustness of its findings in that domain.</p><p>The paper presents simulations and robustness checks to back up its core claims.</p><p>Weaknesses:</p><p>To avoid potential misunderstandings of their work, I think it would be useful for the authors to clarify their statements and implications regarding the utility of item ratings/bids (e-values) in explaining choice behavior. Currently, the paper emphasizes that e-values have limited power to predict choices without explicitly stating the likely reason for this limitation given its own results or pointing out that this limitation is not unique to e-values and would apply to choice outcomes or any other preference elicitation measure too. The core of the paper rests on the argument that the subjective values of the food items are not stored as a relatively constant value, but instead are constructed at the time of choice based on the individual's current state. That is, a food's subjective value is a dynamic creation, and any measure of subjective value will become less accurate with time or new inputs (see Figure 3 regarding choice outcomes, for example). The e-values will change with time, choice deliberation, or other experiences to reflect the change in subjective value. Indeed, most previous studies of choice-induced preference change, including those cited in this manuscript, use multiple elicitations of e-values to detect these changes. It is important to clearly state that this paper provides no data on whether e-values are more or less limited than any other measure of eliciting subjective value. Rather, the paper shows that a static estimate of a food's subjective value at a single point in time has limited power to predict future choices. Thus, a more accurate label for the e-values would be static values because stationarity is the key assumption rather than the means by which the values are elicited or inferred.</p></disp-quote><p>Thank you for this helpful comment. We changed the terminology following the reviewer’s suggestion. The “explicit” values (e-values or ve) are now called “static” values (s-values or vs). Accordingly, we also changed the “Reval” values (r-values or vr) to “dynamic” values (d-values or vd).</p><p>We also address the reviewer's more general point about the utility of item ratings/bids (s-values) and whether our results are likely to hold with other ways of eliciting subjective values. We added a new sub-section in Discussion addressing this and other limitations of our study. To address the reviewer’s point, we write:</p><p>“One limitation of our study is that we only examined tasks in which static values were elicited from explicit reports of the value of food items. It remains to be determined if other ways of eliciting subjective values (e.g., Jensen and Miller, 2010) would lead to similar results. We think so, as the analysis of trials with identical item pairs (Fig. 3) and the difference between forward and backward <italic>Reval</italic> (Fig. 7) are inconsistent with the notion that values are static, regardless of their precise value. It also remains to be determined if our results will generalize to non-food items whose value is less sensitive to satiety and other dynamic bodily states. Perceptual decisions also exhibit sequential dependencies, and it remains to be explored whether these can be explained as a process of value construction, similar to what we propose here for the food-choice task (Gupta et al., 2024; Cho et al., 2002; Zylberberg et al., 2018; Abrahamyan et al., 2016).”</p><disp-quote content-type="editor-comment"><p>There is a puzzling discrepancy between the fits of a DDM using e-values in Figure 1 versus Figure 5. In Figure 1, the DDM using e-values provides a rather good fit to the empirical data, while in Figure 5 its match to the same empirical data appears to be substantially worse. I suspect that this is because the value difference on the x-axis in Figure 1 is based on the e-values, while in Figure 5 it is based on the r-values from the Reval algorithm. However, the computation of the value difference measure on the two x-axes is not explicitly described in the figures or methods section and these details should be added to the manuscript. If my guess is correct, then I think it is misleading to plot the DDM fit to e-values against choice and RT curves derived from r-values. Comparing Figures 1 and 5, it seems that changing the axes creates an artificial impression that the DDM using e-values is much worse than the one fit using r-values.</p></disp-quote><p>We agree with the reviewer that this way of presenting the DDM fits could be misleading. In the previous version of the manuscript, we included the two fits in the same figure panel to make it clear that the sensitivity (slope) of the choice function is greater when we fit the data using the r-values (now d-values) than when we fit them using the e-values (now s-values). In the revised version of Figure 5, we include the data points already shown in Figure 1, so that each DDM fit is shown with their corresponding data points. Thus we avoid giving the false impression that the DDM model fit using the s-values is much worse than the one fit using the d-values. This said, the fit is indeed worse, as we now show with the formal model comparison suggested by the reviewer (next comment).</p><disp-quote content-type="editor-comment"><p>Relatedly, do model comparison metrics favor a DDM using r-values over one using e-values in any of the datasets tested? Such tests, which use the full distribution of response times without dividing the continuum of decision difficulty into arbitrary hard and easy bins, would be more convincing than the tests of RT differences between the categorical divisions of hard versus easy.</p></disp-quote><p>We now include the model comparison suggested by the reviewer. The comparison shows that the DDM model using dynamic values explains the choice and response time data better than one using static values. One potential caveat of this comparison, which explains why we did not include it in the original version of the manuscript, is that the d-values are obtained from a fit to the choice data, which could bias the subsequent DDM comparison. We control for this in three ways: (1) by calculating the difference in Bayesian Information Criterion (BIC) between the models, penalizing the DDM model that uses the d-values for the additional parameter (δ); (2) by comparing the difference in BIC against simulations of a model in which the choice and RT data were obtained assuming static values; this analysis shows that if values were static, the DDM using static values would be favored in the comparison despite having one fewer parameter; (3) ignoring the DDM fit to the choices in the model comparison, and just comparing how well the two models explain the RTs; this comparison is unbiased because the δ values are fit only to the choice data, not the RTs. These analyses are now included in Figure 5 and Figure 5–Figure supplement 2.</p><disp-quote content-type="editor-comment"><p>Revaluation and reduction in the imprecision of subjective value representations during (or after) a choice are not mutually exclusive. The fact that applying Reval in the forward trial order leads to lower deviance than applying it in the backwards order (Figure 7) suggests that revaluation does occur. It doesn't tell us if there is also a reduction in imprecision. A comparison of backwards Reval versus no Reval would indicate whether there is a reduction in imprecision in addition to revaluation. Model comparison metrics and plots of the deviance from the logistic regression fit using e-values against backward and forward Reval models would be useful to show the relative improvement for both forms of Reval.</p></disp-quote><p>We agree with the reviewer that the occurrence of revaluation does not preclude other factors from affecting valuation. Following the reviewer’s suggestion we added a panel to Figure 6 (new panel B), in which we show the change in the deviance from the logistic regression fits between <italic>Reval</italic> (forward direction) and <italic>no-Reval</italic>. The figure clearly shows that the difference in deviance for the data is much larger than that obtained from simulations of choice data generated from the logistic fits to the static values (shown in red).</p><p>Interestingly, we also observe that the deviance obtained after applying Reval in the backward direction is lower than that obtained using the s-values. We added a panel to figure 7 showing this (Fig. 7B). This observation, however, does not imply that there are factors affecting valuation besides revaluation (e.g.,”reduction in imprecision”). Indeed, as we now show in a new panel in Figure 11 (panel F), the same effect (lower deviance for backward Reval than no-Reval) is observed in simulations of the <italic>ceDDM</italic>.</p><p>Besides the new figure panels (Fig. 6B, 7B, 11F), we mention in Discussion (new subsection, “Limitations...”, paragraph #2) the possibility that there are other non-dynamic contributions to the reduction in deviance for Backward Reval compared to no-Reval:</p><p>“Another limitation of our study is that, in one of the datasets we analyzed (Sepulveda et al. 2020), applying <italic>Reval</italic> in the forward direction was no better than applying it in the backward direction (Fig. 10). We speculate that this failure is related to idiosyncrasies of the experimental design, in particular, the use of alternating blocks of trials with different instructions (select preferred vs. select non-preferred). More importantly, <italic>Reval</italic> applied in the backward direction led to a significant reduction in deviance relative to that obtained using the static values. This reduction was also observed in the ceDDM, suggesting that the effect may be explained by the changes in valuation during deliberation. However, we cannot discard a contribution from other, non-dynamic changes in valuation between the rating and choice phase including contextual effects (Lichtenstein and Slovic, 2006), stochastic variability in explicit value reporting (Polania et al., 2019), and the limited range of numerical scales used to report value.”</p><disp-quote content-type="editor-comment"><p>Did the analyses of BOLD activity shown in Figure 9 orthogonalize between the various e-valueand r-value-based regressors? I assume they were not because the idea was to let the two types of regressors compete for variance, but orthogonalization is common in fMRI analyses so it would be good to clarify that this was not used in this case. Assuming no orthogonalization, the unique variance for the r-value of the chosen option in a model that also includes the e-value of the chosen option is the delta term that distinguishes the r and e-values. The delta term is a scaled count of how often the food item was chosen and rejected in previous trials. It would be useful to know if the vmPFC BOLD activity correlates directly with this count or the entire r-value (e-value + delta). That is easily tested using two additional models that include only the r-value or only the delta term for each trial.</p></disp-quote><p>We did not orthogonalize the static value and dynamic value regressors. We have included this detail in the revised methods. We thank the reviewer for the suggestion to run additional models to improve our ability to interpret our findings. We have substantially revised all fMRI-related sections of the paper. We took this opportunity to apply standardized and reproducible preprocessing steps implemented in <italic>fmriprep</italic>, present whole-brain corrected maps on a reconstructed surface of a template brain, and include links to the full statistical maps for the reader to navigate the full map, rather than rely on the static image in the figures. We implemented four models in total: model 1 includes both static value (Vs) obtained during the auction procedure prior to the choice phase and dynamic value (Vd) output by the revaluation algorithm (similar to the model presented in the first submission); model 2 includes only delta = Vd - Vs; model 3 includes only Vs; model 4 includes only Vd. All models included the same confound and nuisance regressors. We found that Vd was positively related to BOLD in vmPFC when accounting for Vs, correcting for familywise error rate at the whole brain level. Interestingly, the relationship between delta and vmPFC BOLD did not survive whole-brain correction and the effect size of the relationship between Vd and vmPFC bold in model 4 was larger than the effect size of the relationship between Vs and vmPFC bold in model 3 and survived correction at the whole brain level encompassing more of the vmPFC. Together, these findings bolster our claim that Vd better accounts for BOLD variability in vmPFC, a brain region reliably linked to valuation.</p><disp-quote content-type="editor-comment"><p>Please confirm that the correlation coefficients shown in Figure 11 B are autocorrelations in the MCMC chains at various lags. If this interpretation is incorrect, please give more detail on how these coefficients were computed and what they represent.</p></disp-quote><p>We added a paragraph in Methods explaining how we compute the correlations in Figure 11B (last paragraph of the sub-section “Correlated-evidence DDM” in Methods):</p><p>“The correlations in Fig. 11B were generated using the best-fitting parameters for each participant to simulate 100,000 Markov chains. We generate Markov chain samples independently for the left and right items over a 1-second period. To illustrate noise correlations, the simulations assume that the static value of both the left and right items is zero. We then and for each of the Markov chains (𝑥). Pearson's𝑥 correlation is computed between these 𝑡 calculate the difference in dynamic value (𝑥) between the left and right items at each time (𝑡) differences at time zero, 𝑥𝑖(𝑡 = 0), and at time 𝑥𝑖(𝑡 = τ), for different time lags τ. Correlations were calculated independently for each participant. Each trace in Fig. 11B represents a different participant.”</p><disp-quote content-type="editor-comment"><p>The paper presents the ceDDM as a proof-of-principle type model that can reproduce certain features of the empirical data. There are other plausible modifications to bounded evidence accumulation (BEA) models that may also reproduce these features as well or better than the ceDDM. For example, a DDM in which the starting point bias is a function of how often the two items were chosen or rejected in previous trials. My point is not that I think other BEA models would be better than the ceDDM, but rather that we don't know because the tests have not been run. Naturally, no paper can test all potential models and I am not suggesting that this paper should compare the ceDDM to other BEA processes. However, it should clearly state what we can and cannot conclude from the results it presents.</p></disp-quote><p>Indeed, the <italic>ceDDM</italic> should be interpreted as a proof-of-principle model, which shows that drifting values can explain many of our results. It is definitely wrong in the details, and we are open to the possibility that a different way of introducing sequential dependencies between decisions may lead to a better match to the experimental data. We now mention this in a new subsection of Discussion, “Limitations...” paragraph #3:</p><p>“Finally, we emphasize that the <italic>ceDDM</italic> should be interpreted as a proof-of-principle model used to illustrate how stochastic fluctuations in item desirability can explain many of our results. We chose to model value changes following an MCMC process. However, other stochastic processes or other ways of introducing sequential dependencies (e.g., variability in the starting point of evidence accumulation) may also explain the behavioral observations. Furthermore, there likely are other ways to induce changes in the value of items other than through past decisions. For example, attentional manipulations or other experiences (e.g., actual food consumption) may change one's preference for an item. The current version of the <italic>ceDDM</italic> does not allow for these influences on value, but we see no fundamental limitation to incorporating them in future instantiations of the model.”</p><disp-quote content-type="editor-comment"><p>This work has important practical implications for many studies in the decision sciences that seek to understand how various factors influence choice outcomes. By better accounting for the context-specific nature of value construction, studies can gain more precise estimates of the effects of treatments of interest on decision processes.</p></disp-quote><p>Thank you!</p><disp-quote content-type="editor-comment"><p>That said, there are limitations to the generalizability of these findings that should be noted.</p><p>These limitations stem from the fact that the paper only analyzes choices between food items and the outcomes of the choices are not realized until the end of the study (i.e., participants do not eat the chosen item before making the next choice). This creates at least two important limitations. First, preferences over food items may be particularly sensitive to mindsets/bodily states. We don't yet know how large the choice deltas may be for other types of goods whose value is less sensitive to satiety and other dynamic bodily states. Second, the somewhat artificial situation of making numerous choices between different pairs of items without receiving or consuming anything may eliminate potential decreases in the preference for the chosen item that would occur in the wild outside the lab setting. It seems quite probable that in many real-world decisions, the value of a chosen good is reduced in future choices because the individual does not need or want multiples of that item. Naturally, this depends on the durability of the good and the time between choices. A decrease in the value of chosen goods is still an example of dynamic value construction, but I don't see how such a decrease could be produced by the ceDDM.</p></disp-quote><p>These are all great points. The question of how generalizable our results are to other domains is wide open. We do have preliminary evidence suggesting that in a perceptual decision-making task with two relevant dimensions (motion and color; Kang, Loffler et al. eLife 2021), the dimension that was most informative to resolve preference in the past is prioritized in future decisions. We believe that a similar process underlies the apparent change in value in value-based decisions. We decided not to include this experiment in the manuscript, as it would make the paper much longer and the experimental designs are very different. Exploring the question of generality is a matter for future studies.</p><p>We also agree that food consumption is likely to change the value of the items. For example, after eating something salty we are likely to want something to drink. We mention in the revised manuscript that time, choice deliberation, attentional allocation and other experiences (including food consumption) are likely to change the value of the alternatives and thus affect future choices and valuations.</p><p>The <italic>ceDDM</italic> captures only sequential dependencies that can be attributed to values that undergo diffusion-type changes during deliberation. While the ceDDM captures many of the experimental observations, the value of an item may change for reasons not captured by the <italic>ceDDM</italic>. For example, food consumption is likely to change the value of items (e.g., wanting something to drink after eating something salty). The reviewer is correct that the current version of <italic>ceDDM</italic> could not account for these changes in value. However, we see no fundamental limitation to extending the <italic>ceDDM</italic> to account for them.</p><p>We discuss these issues in a new subsection in Discussion (“Limitations...” paragraph #3).</p><disp-quote content-type="editor-comment"><p><bold>Recommendations for the authors:</bold></p><p><bold>Reviewer #1 (Recommendations For The Authors):</bold></p><p>Summary</p><p>The authors address assumptions of bounded accumulation of evidence for value-based decision-making. They provide convincing evidence that subjects drift in their subjective preferences across time and demonstrate valuable methods to detect these drifts in certain task designs.</p><p>My specific comments are intended to assist the authors with making the paper as clear as possible. My only major concern is with the reporting of the fMRI results.</p></disp-quote><p>Thank you, please see our responses above for a description of the changes we made to the fMRI analyses.</p><disp-quote content-type="editor-comment"><p>Specific comments</p><p>- In the intro, I would ask the authors to consider the idea that things like slow drift in vigilance/motivation or faster drifts in spatial attention could also generate serial dependencies in perceptual tasks. I think the argument that these effects are larger in value-based tasks is reasonable, but the authors go a bit too far (in my opinion) arguing that similar effects do not exist *at all* in perceptual decision-making.</p></disp-quote><p>We added a sentence in the Discussion (new section on Limitations, paragraph #1) mentioning some of the literature on sequential dependencies in perceptual tasks and asking whether there might be a common explanation for such dependencies for perceptual and value-based decisions. We tried including this in the Introduction, but we thought it disrupted the flow too much.</p><disp-quote content-type="editor-comment"><p>- Figure 1: would it not be more clear to swap the order of panels A and B? Since B comes first in the task?</p></disp-quote><p>We agree, we swapped the order of panels A and B.</p><disp-quote content-type="editor-comment"><p>- Figure 2: the label 'simulations' might be better as 'e-value simulations'</p></disp-quote><p>Yes, we changed the label ‘simulations’ to ‘simulations with s-values’ (we changed the term <italic>explicit</italic> value to <italic>static</italic> value, following a suggestion by Reviewer #2).</p><disp-quote content-type="editor-comment"><p>- For the results related to Figure 2, some citations related to gaps between &quot;stated versus revealed preferences&quot; seem appropriate.</p></disp-quote><p>We added a few relevant citations where we explain the results related to Figure 2.</p><disp-quote content-type="editor-comment"><p>- Figure 3: in addition to a decrease in match preferences over the session, it would be nice to look at other features of the task which might have varied over the session. e.g. were earlier trials more likely to be predicted by e-value?</p></disp-quote><p>We do see a trend in this direction, but the effect is not significant. The following figure shows the consistency of the choices with the stated values, as a function of the |∆value|, for the first half (blue) and the second half (red) of the trials. The x-axis discretizes the absolute value of the difference in static value between the left and right items, binned in 17 bins of approximately equal number of trials.</p><fig id="sa3fig1" position="float"><label>Author response image 1.</label><graphic mimetype="image" mime-subtype="tiff" xlink:href="elife-96997-sa3-fig1-v1.tif"/></fig><p>The slope is shallower for the second half, but a logistic regression model revealed that the difference is not significant:<disp-formula id="sa3equ1">,<mml:math id="sa3m1"><mml:mrow><mml:mi>logit</mml:mi><mml:mo>⁡</mml:mo><mml:mrow><mml:mo>[</mml:mo><mml:msub><mml:mi>p</mml:mi><mml:mrow><mml:mtext>consistent</mml:mtext></mml:mrow></mml:msub><mml:mo>]</mml:mo></mml:mrow><mml:mo>=</mml:mo><mml:msub><mml:mi>β</mml:mi><mml:mrow><mml:mn>0</mml:mn></mml:mrow></mml:msub><mml:mo>+</mml:mo><mml:msub><mml:mi>β</mml:mi><mml:mrow><mml:mn>1</mml:mn></mml:mrow></mml:msub><mml:mrow><mml:mo>|</mml:mo><mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow><mml:mi>s</mml:mi></mml:mrow></mml:msub></mml:mrow><mml:mo>|</mml:mo></mml:mrow><mml:mo>+</mml:mo><mml:msub><mml:mi>β</mml:mi><mml:mrow><mml:mn>2</mml:mn></mml:mrow></mml:msub><mml:mrow><mml:mo>|</mml:mo><mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>v</mml:mi><mml:mrow><mml:mi>s</mml:mi></mml:mrow></mml:msub></mml:mrow><mml:mo>|</mml:mo></mml:mrow><mml:mo>×</mml:mo><mml:msub><mml:mi>I</mml:mi><mml:mrow><mml:mtext>late </mml:mtext></mml:mrow></mml:msub></mml:mrow></mml:math></disp-formula></p><p>where Ilate is an indicator variable that takes a value of 1 for the second half of the trials and zero otherwise.</p><p>As expected from the figure β2 was negative (-0.15) but the effect was not significant (p-value = 0.32, likelihood ratio test).</p><p>We feel we do not have much to say about this result, which may be due to lack of statistical power, so we would rather not include this analysis in the revised manuscript.</p><p>It is worth noting that if we repeat the analysis using the dynamic values obtained from Reval instead of the static values, the consistency is overall much greater and little difference is observed between the first and second halves of the experiment:</p><fig id="sa3fig2" position="float"><label>Author response image 2.</label><graphic mimetype="image" mime-subtype="tiff" xlink:href="elife-96997-sa3-fig2-v1.tif"/></fig><disp-quote content-type="editor-comment"><p>- The e-value DDM fit in Figure 1C/D goes through the points pretty well, but the e-value fits in 5A do not because of a mismatch with the axis. The x-axis needs to say whether the value difference is the e-value or the r-value. Also, it seems only fair to plot the DDM for the r-value on a plot with the x-axis being the e-value.</p></disp-quote><p>Thank you for this comment, we have now changed Figure 5A, such that both sets of data points are shown (data grouped by both e-values and by r-values). We agree that the previous version made it seem as if the fits were worse for the DDM fit to the e-values. The fits are indeed worse, as revealed by a new DDM model comparison (Figure 5–Figure supplement 2), but the effect is more subtle than the previous version of the figure implied.</p><disp-quote content-type="editor-comment"><p>- How is Figure 5B &quot;model free&quot; empirical support? The fact that the r-value model gives better separation of the RTs on easy and hard trials doesn't seem &quot;model-free&quot; and also it isn't clear how this directly relates to being a better model. It seems that just showing a box-plot of the R2 for the RT of the two models would be better?</p></disp-quote><p>We agree that “model free” may not be the best expression, since the r-values (now d-values) are derived from a model (Reval). Our intention was to make clear that because Reval only depends on the choices, the relationship between RT and ∆vdynamic is a prediction. We no longer use the term, model free, in the caption. We tried to clarify the point in Results, where we explain this figure panel. We have also included a new model comparison (Figure 5–Figure supplement 2), showing that the DDM model fit to the d-values explains choice and RT better than one fit to the s-values.</p><p>This said, we do consider the separation in RTs between easy and hard trials to be a valid metric to compare the accuracy of the static and dynamic values. The key assumption is that there is a monotonically decreasing relationship between value difference, ∆v, and response time. The monotonic relationship does not need to hold for individual trials (due to the noisiness of the RTs) but should hold if one were to average a large enough number of trials for each value of ∆v.</p><p>Under this assumption, the more truthful a value representation is (i.e., the closer the value we infer is to the true subjective value of the item on a given trial, assuming one exists), the greater the difference in RTs between trials judged to be difficult and those considered easy. To illustrate this with an extreme case, if an experimenter’s valuation of the items is very inaccurate (e.g., done randomly), then on average there will be no difference between easy and difficult RTs as determined by this scoring.</p><disp-quote content-type="editor-comment"><p>- Line 189: Are the stats associated with Eq 7, was the model fit subject by subject? Combining subjects? A mixed-effects model? Why not show a scatter plot of the coefficients of Δvₑ and Δvᵣ (1 point/subject).</p></disp-quote><p>The model was not fit separately for each subject. Instead, we concatenated trials from all subjects, allowing each subject to have a different bias term (β0,i).</p><p>We have now replaced it with the analysis suggested by the reviewer. We fit the logistic regression model independently for each participant. The scatter plot suggested by the reviewer is shown in Figure 5–Figure supplement 1. Error bars indicate the s.e. of the regression coefficients:</p><p>It can be seen that the result is consistent with what we reported before: βd is significantly positive for all participants, while βs is not.</p><disp-quote content-type="editor-comment"><p>- I think Figure S1 should be a main figure.</p></disp-quote><p>Thank you for this suggestion, we have now included the former Figure S1 as an additional panel in Figure 5.</p><disp-quote content-type="editor-comment"><p>- Fig 9 figure and text (line 259) don't exactly match. In the text it says that the BOLD correlated with vᵣ and not vₑ, but the caption says there were correlations with vᵣ after controlling for vₑ. Is there really nothing in the brain that correlated with vₑ? This seems hard to believe given how correlated the two estimates are. In the methods, 8 regressors are described. A more detailed description of the results is needed.</p></disp-quote><p>Thank you for pointing out the inconsistency in our portrayal of the results in the main text and in the figure caption. We have substantially revised all fMRI methods, re-ran fMRI data preprocessing and implemented new, simpler, and more comprehensive GLM models following Reviewer #2's suggestion. Consequently, we have replaced Figure 9, added Figure 9 — Figure Supplement 1, and uploaded all maps to NeuroVault. These new models and maps allow for a clearer interpretation of our findings. More details about the fMRI analyses in the methods and results are included in the revision. We took care to use similar language in the main text and in the figure captions to convey the results and interpretation. The new analyses strengthen our original conclusion: dynamic values better explain BOLD activity in the ventromedial prefrontal cortex, a region consistently associated with valuation, than static values.</p><disp-quote content-type="editor-comment"><p>- It's great that the authors reanalyzed existing datasets (fig 10). I think the ΔRT plots are the least clear way to show that _reval_ is better. Why not a figure like Figure 6a and Figure 7 for the existing datasets?</p></disp-quote><p>We agree with the reviewer. We have replaced Fig. 10 with a more detailed version. For each dataset, we show the ΔRT plots, but we also show figures equivalent to Fig. 6a, Fig. 7a, and the new Fig. 6b (Deviance with and without <italic>Reval</italic>).</p><disp-quote content-type="editor-comment"><p><bold>Reviewer #2 (Recommendations For The Authors):</bold></p><p>I assume that the data and analysis code will be made publicly and openly available once the version of record is established.</p></disp-quote><p>Yes, the data and analysis code is now available at: <ext-link ext-link-type="uri" xlink:href="https://github.com/arielzylberberg/Reval_eLife_2024">https://github.com/arielzylberberg/Reval_eLife_2024</ext-link></p><p>We added a Data Availability statement to the manuscript.</p></body></sub-article></article>